chr1:11845780:> Detail (hg19)

Information

Genome

Assembly Position
hg19 chr1:11,845,780-11,866,021
hg38 chr1:11,785,723-11,805,964 

HGVS

Type Transcript Protein
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

[No Data.]

ClinVar

Clinical Significance
Review star [No Data.]
Show details
Links
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.050 squamous cell carcinoma NA BeFree,GAD,LHGDN Detail
0.003 Carcinoma, Transitional Cell NA BeFree,GAD Detail
0.245 Cardiovascular Diseases The aim was to examine the association and effect modification by serum folate a... BeFree,CTD_human,GAD,LHGDN 24458267 Detail
0.015 Carotid Artery Diseases NA GAD,LHGDN Detail
0.008 carotid stenosis NA BeFree,GAD,LHGDN Detail
0.006 celiac disease Pathogenic predisposing avenues increasing the hypercoagulability in celiac dise... BeFree,GAD 25149392 Detail
0.005 Neoplastic Cell Transformation NA GAD Detail
0.005 intracranial aneurysm NA BeFree,GAD Detail
0.002 Cerebral Arterial Diseases NA GAD Detail
<0.001 cerebral atherosclerosis NA BeFree Detail
0.013 cerebral infarction The methylenetetrahydrofolate reductase (MTHFR) 677C>T and 1298A>C polymorphisms... BeFree,GAD 25098357 Detail
0.201 brain ischemia NA CTD_human,GAD,LHGDN Detail
0.011 Transient ischemic attack NA BeFree,GAD Detail
0.007 cerebral palsy NA BeFree,GAD Detail
0.024 Cerebrovascular Disorders NA GAD Detail
0.006 Malignant tumor of cervix MTHFR/p53 polymorphisms as genetic factors for cervical intraepithelial neoplasi... BeFree 24474455 Detail
<0.001 Cervix Diseases NA BeFree Detail
<0.001 Cervical dysplasia NA BeFree Detail
0.137 Uterine Cervical Neoplasm NA CTD_human,GAD Detail
<0.001 Developmental Disabilities NA BeFree Detail
0.005 Choline Deficiency NA GAD Detail
0.005 chondrosarcoma NA BeFree,GAD,LHGDN Detail
0.002 chorioamnionitis NA GAD Detail
0.002 hemophilia B NA GAD Detail
0.009 Chromosome Aberrations NA GAD Detail
<0.001 Congenital chromosomal disease NA BeFree Detail
0.002 Chromosome Deletion NA GAD Detail
0.181 cleft lip NA BeFree,CTD_human,GAD,LHGDN Detail
0.048 cleft palate NA BeFree,GAD Detail
0.123 Congenital clubfoot NA BeFree,CTD_human,GAD Detail
<0.001 Cluster Headache NA BeFree Detail
0.021 ulcerative colitis NA BeFree,GAD,LHGDN Detail
0.163 Colonic Neoplasms NA BeFree,CTD_human,GAD,LHGDN Detail
0.203 Colorectal Neoplasms NA BeFree,CTD_human,GAD,LHGDN Detail
0.002 Connective Tissue Diseases NA GAD Detail
0.002 Constipation NA GAD Detail
0.046 Coronary Arteriosclerosis Methylenetetrahydrofolate reductase C677T polymorphism is associated with increa... BeFree,GAD 26095803 Detail
0.239 Coronary heart disease These preliminary findings indicate that these two MTHFR genetic polymorphisms a... BeFree,CTD_human,GAD,LHGDN 24720776 Detail
0.239 Coronary heart disease In the maternal analysis, the MTHFR C677T polymorphism was significantly associa... BeFree,CTD_human,GAD,LHGDN 25256053 Detail
0.239 Coronary heart disease Our results support the MTHFR -677T allele as a susceptibility factor for CHD in... BeFree,CTD_human,GAD,LHGDN 25472587 Detail
0.239 Coronary heart disease Results from this study indicate that the MTHFR c.1625A>C genetic variant influe... BeFree,CTD_human,GAD,LHGDN 25494855 Detail
0.239 Coronary heart disease Methylenetetrahydrofolate reductase C677T polymorphism is associated with increa... BeFree,CTD_human,GAD,LHGDN 26095803 Detail
0.010 Crohn Disease NA BeFree,GAD Detail
<0.001 Cytomegalovirus Infections NA BeFree Detail
0.002 Deafness NA GAD Detail
0.137 Hearing Loss, Sudden NA CTD_human,GAD,LHGDN Detail
0.002 Presenile dementia NA BeFree Detail
<0.001 Senile dementia NA BeFree Detail
0.007 Dementia, Vascular NA BeFree,GAD Detail
0.002 Demyelinating Diseases NA GAD Detail
0.020 Mental Depression Significance of dietary folate intake, homocysteine levels and MTHFR 677 C>T gen... BeFree,GAD 24532086 Detail
0.020 Mental Depression Genetic polymorphisms of methylenetetrahydrofolate reductase (MTHFR) gene and su... BeFree,GAD 26177556 Detail
0.126 depressive disorder Significance of dietary folate intake, homocysteine levels and MTHFR 677 C>T gen... BeFree,CTD_human 24532086 Detail
0.126 depressive disorder Genetic polymorphisms of methylenetetrahydrofolate reductase (MTHFR) gene and su... BeFree,CTD_human 26177556 Detail
0.120 Drug Eruptions NA CTD_human Detail
0.080 Diabetes Mellitus, Experimental NA RGD Detail
0.015 Diabetes Mellitus, Insulin-Dependent NA BeFree,GAD Detail
0.132 Diabetic Angiopathies NA BeFree,CTD_human,GAD Detail
0.003 Diabetic Neuropathies NA BeFree,GAD Detail
0.015 diabetic retinopathy Genetic variants in ICAM1, PPARGC1A and MTHFR are potentially associated with di... BeFree,GAD,LHGDN 25324196 Detail
0.003 diarrhea NA BeFree,GAD Detail
0.002 discrete subaortic stenosis NA GAD Detail
0.005 Dislocations NA GAD,LHGDN Detail
0.021 DNA Damage NA GAD Detail
0.239 Down syndrome Meta-analysis of Methylenetetrahydrofolate reductase maternal gene in Down syndr... BeFree,CTD_human,GAD,LHGDN 24913031 Detail
0.239 Down syndrome Maternal methylenetetrahydrofolate reductase C677T polymorphism and down syndrom... BeFree,CTD_human,GAD,LHGDN 25265565 Detail
0.239 Down syndrome The frequency of the MTHFR 677C allele in DS mothers (79.8%) was significantly h... BeFree,CTD_human,GAD,LHGDN 25671679 Detail
<0.001 Drug habituation NA BeFree Detail
0.002 drug allergy NA GAD Detail
0.007 Drug toxicity NA GAD Detail
<0.001 Dry Eye Syndromes Also, it is determined an association between MTHFR C677T polymorphism and feeli... BeFree 25824380 Detail
0.003 patent ductus arteriosus NA BeFree,GAD Detail
<0.001 Dyspnea NA BeFree Detail
0.008 eclampsia The mechanisms may include the following pathways: [TGFB1 or TNFA]-[IL1B]-[pre-e... BeFree,GAD 25879409 Detail
<0.001 Eczema NA BeFree Detail
0.005 Edema NA GAD Detail
0.002 Ehlers-Danlos syndrome NA GAD Detail
0.003 encephalomalacia NA LHGDN Detail
0.122 Endometrial Neoplasms NA CTD_human,GAD Detail
0.023 epilepsy A difference in the methylation levels of methylenetetrahydrofolate reductase (M... BeFree,GAD,LHGDN 25915064 Detail
0.002 Epistaxis NA GAD Detail
0.002 Escherichia coli Infections NA GAD Detail
0.002 Esophageal and Gastric Varices NA GAD Detail
0.033 Esophageal Neoplasms NA BeFree,GAD,LHGDN Detail
0.012 Fatty Liver NA BeFree,GAD Detail
0.002 Femur Head Necrosis NA GAD Detail
0.002 Fetal Death NA GAD Detail
0.007 Fetal Diseases NA GAD Detail
0.017 Fetal Growth Retardation NA GAD Detail
0.005 Fetal Membranes, Premature Rupture NA GAD Detail
<0.001 breast fibrocystic disease NA BeFree Detail
<0.001 fibromyalgia Angiotensin converting enzyme and methylenetetrahydrofolate reductase gene varia... BeFree 25824380 Detail
0.002 Fibrosis NA GAD Detail
0.064 Folic Acid Deficiency NA BeFree,GAD Detail
0.005 Foramen Ovale, Patent NA BeFree,GAD Detail
0.002 Pathological fracture NA GAD Detail
0.003 Gastritis, Atrophic NA BeFree,GAD Detail
0.125 Gastrointestinal Diseases NA CTD_human,GAD Detail
0.005 Gastrointestinal Hemorrhage NA GAD Detail
0.007 Gastrointestinal Neoplasms NA GAD Detail
0.005 Gaucher disease NA BeFree,GAD Detail
0.002 Female Genital Diseases NA GAD Detail
0.008 glaucoma The present investigation on MTHFR C677T and glaucoma reveals that the TT genoty... BeFree,GAD 25054348 Detail
0.008 Angle Closure Glaucoma NA BeFree,GAD,LHGDN Detail
<0.001 primary angle-closure glaucoma Ours is the first report demonstrating association of MTHFR C677T with POAG but ... BeFree 25054348 Detail
0.009 glioblastoma NA BeFree,GAD,LHGDN Detail
0.006 Glioma NA BeFree,GAD Detail
<0.001 membranous glomerulonephritis NA BeFree Detail
0.003 Focal glomerulosclerosis NA BeFree,GAD Detail
0.143 Graft-vs-Host Disease NA BeFree,CTD_human,GAD,LHGDN Detail
0.003 Graves Disease NA BeFree,GAD Detail
0.012 Head and Neck Neoplasms NA GAD Detail
<0.001 Headache NA BeFree Detail
0.002 Hearing Loss, Partial NA GAD Detail
0.008 Sensorineural Hearing Loss (disorder) NA BeFree,GAD Detail
<0.001 cardiac arrest NA BeFree Detail
0.168 congenital heart defects Studies have reported that the MTHFR C677T polymorphism was associated with the ... BeFree,CTD_human,GAD,LHGDN 25256053 Detail
0.008 Heart Diseases NA BeFree,GAD Detail
0.002 Heart Septal Defects NA GAD Detail
0.003 Atrial Septal Defects NA BeFree,GAD Detail
0.132 Hematological Disease NA CTD_human,GAD,LHGDN Detail
<0.001 hemochromatosis NA BeFree Detail
0.007 hemolytic-uremic syndrome NA BeFree,GAD Detail
0.008 Hemophilia A NA BeFree,GAD Detail
0.002 Hemorrhage NA GAD Detail
<0.001 Hepatic Vein Thrombosis NA BeFree Detail
<0.001 hepatitis NA BeFree Detail
<0.001 hepatitis A NA BeFree Detail
0.003 hepatitis B In conclusion, thrombo and fibro-genetic mechanisms of PAI-1 4G-4G and MTHFR 677... BeFree,GAD 25987440 Detail
0.003 Hepatitis, Chronic NA BeFree,GAD Detail
0.002 Hepatitis, Toxic NA GAD Detail
0.004 hepatitis C NA BeFree,LHGDN Detail
0.002 HIV Infections NA GAD Detail
0.003 Hodgkin Disease NA BeFree,GAD Detail
0.006 homocystinuria NA BeFree,GAD Detail
0.008 Huntington disease NA BeFree,GAD,LHGDN Detail
0.008 Hypercholesterolemia NA BeFree,GAD Detail
0.006 Hypercholesterolemia, Familial NA BeFree,GAD Detail
0.006 hyperglycemia A significant association was observed between the MTHFR 677T allele and increas... BeFree,GAD,LHGDN 25429430 Detail
0.012 Hyperlipidemia NA BeFree,GAD Detail
0.005 Hyperplasia NA GAD Detail
0.120 Hypersensitivity NA CTD_human Detail
0.005 Immediate hypersensitivity NA GAD Detail
0.003 pulmonary hypertension Variants in methylenetetrahydrofolate reductase are common in the general popula... BeFree,GAD 25304246 Detail
0.082 hyperthyroidism NA GAD,RGD Detail
0.080 hypothyroidism NA RGD Detail
0.002 Neonatal disorder NA GAD Detail
0.003 Infarction NA LHGDN Detail
0.005 infertility NA GAD Detail
0.127 Female infertility NA CTD_human,GAD Detail
0.012 Inflammation NA GAD Detail
0.017 Inflammatory Bowel Diseases NA BeFree,GAD Detail
0.007 Insulin resistance NA GAD Detail
0.003 intermittent claudication NA BeFree,GAD Detail
0.008 ischemia NA BeFree,GAD Detail
0.135 Kidney Diseases A total of 40 male patients with CKD and stable renal function (Kidney Disease O... BeFree,CTD_human,GAD 24711158 Detail
0.063 Kidney Failure, Chronic NA BeFree,GAD,LHGDN Detail
0.002 Kidney Neoplasm NA GAD Detail
0.007 Premature Obstetric Labor NA GAD Detail
0.005 Laryngeal neoplasm NA GAD Detail
0.002 Lead Poisoning NA GAD Detail
0.003 Legg-Calve-Perthes disease NA BeFree,GAD Detail
0.001 vascular disease occlusive All subjects were genotyped for 13 polymorphic variants in the genes of xenobiot... BeFree 23107763 Detail
0.047 leukemia NA BeFree,GAD,LHGDN Detail
0.135 chronic lymphocytic leukemia NA BeFree,CTD_human,GAD,LHGDN Detail
0.005 lymphoid leukemia NA BeFree,GAD Detail
0.031 Leukemia, Lymphocytic, Acute, L1 These findings confirm that the MTHFR C677T polymorphism could be considered as ... BeFree,GAD 24637499 Detail
0.031 Leukemia, Lymphocytic, Acute, L1 MTHFR (677 and 1298) genotype of children with ALL and healthy adult controls we... BeFree,GAD 24919644 Detail
0.031 Leukemia, Lymphocytic, Acute, L1 The association between methylenetetrahydrofolate reductase C677 > T polymorphis... BeFree,GAD 25450284 Detail
0.031 Leukemia, Lymphocytic, Acute, L1 Lack of association between polymorphisms in genes MTHFR and MDR1 with risk of c... BeFree,GAD 25520092 Detail
0.031 Leukemia, Lymphocytic, Acute, L1 Moreover, significantly decreased susceptibility to ALL was observed for MTHFR T... BeFree,GAD 25746326 Detail
0.031 Leukemia, Lymphocytic, Acute, L1 Our results indicated that the MTHFR C677T T allele was a protective biomarker f... BeFree,GAD 25793509 Detail
0.002 Leukemia, Lymphocytic, Acute, L2 NA GAD Detail
0.337 hyperhomocysteinemia All subjects were genotyped for 13 polymorphic variants in the genes of xenobiot... BeFree 23107763 Detail
0.017 Leukemia, Myelocytic, Acute Methylenetetrahydrofolate reductase gene polymorphisms contribute to acute myelo... BeFree,GAD,LHGDN 25080853 Detail
0.004 myeloid leukemia NA BeFree,LHGDN Detail
0.021 Myeloid Leukemia, Chronic Methylenetetrahydrofolate reductase gene polymorphisms contribute to acute myelo... BeFree,GAD,LHGDN 25080853 Detail
0.021 Myeloid Leukemia, Chronic The methylenetetrahydrofolate reductase (MTHFR) 677 C>T polymorphism increases t... BeFree,GAD,LHGDN 25510667 Detail
0.002 Precursor B-Cell Lymphoblastic Leukemia-Lymphoma NA GAD Detail
0.002 Adult T-Cell Lymphoma/Leukemia NA GAD Detail
0.124 leukopenia NA BeFree,CTD_human,GAD Detail
0.026 liver cirrhosis In conclusion, thrombo and fibro-genetic mechanisms of PAI-1 4G-4G and MTHFR 677... BeFree,GAD,LHGDN 25987440 Detail
0.007 Liver Cirrhosis, Alcoholic NA BeFree,GAD Detail
0.130 Liver diseases NA BeFree,CTD_human,GAD Detail
0.002 Alcoholic Liver Diseases NA GAD Detail
0.097 Liver neoplasms NA GAD,LHGDN,RGD Detail
0.005 Chronic Obstructive Airway Disease NA GAD Detail
0.133 Lung Neoplasms NA CTD_human,GAD,LHGDN Detail
<0.001 Lupus Vulgaris NA BeFree Detail
<0.001 Lupus Erythematosus, Discoid NA BeFree Detail
0.107 colorectal cancer Further SNPs associated with CRC risk included several previously reported to be... BeFree 17000706 Detail
0.026 colorectal carcinoma Further SNPs associated with CRC risk included several previously reported to be... BeFree 17000706 Detail
0.011 Lupus Erythematosus, Systemic NA BeFree,GAD Detail
0.002 Lymphatic Metastasis NA GAD Detail
0.144 lymphoma NA BeFree,CTD_human,GAD,LHGDN Detail
0.126 Lymphoma, Follicular NA BeFree,CTD_human,GAD Detail
0.010 Lymphoproliferative Disorders NA BeFree,GAD Detail
0.146 Homocysteinemia All subjects were genotyped for 13 polymorphic variants in the genes of xenobiot... BeFree 23107763 Detail
<0.001 malaria NA BeFree Detail
0.002 Malaria, Falciparum NA GAD Detail
<0.001 Primary malignant neoplasm of liver NA BeFree Detail
0.002 Animal Mammary Neoplasms NA GAD Detail
0.003 Marfan syndrome NA BeFree,GAD Detail
0.002 Marijuana Abuse NA GAD Detail
0.057 Malignant neoplasm of lung SNPs in MTRR (rs13162612; OR = 0.25; 95% CI: 0.11-0.58; rs10512948; OR = 0.61; 9... BeFree 23372658 Detail
0.007 Carcinoma of lung SNPs in MTRR (rs13162612; OR = 0.25; 95% CI: 0.11-0.58; rs10512948; OR = 0.61; 9... BeFree 23372658 Detail
<0.001 melanoma NA BeFree Detail
0.002 Meningeal Neoplasms NA GAD Detail
0.011 meningioma NA BeFree,GAD,LHGDN Detail
0.126 Meningomyelocele NA BeFree,CTD_human,GAD Detail
<0.001 premature menopause NA BeFree Detail
0.006 Mental Retardation NA BeFree,GAD Detail
0.002 mesenteric vascular occlusion NA GAD Detail
0.002 Mesothelioma NA GAD Detail
0.007 Metabolic Diseases NA BeFree,GAD Detail
<0.001 Microangiopathy, Diabetic NA BeFree Detail
0.002 Mouth Abnormalities NA GAD Detail
0.012 Mouth Neoplasms NA GAD Detail
<0.001 Moyamoya disease The roles of methylenetetrahydrofolate reductase 677C>T and 1298A>C polymorphism... BeFree 25098357 Detail
0.021 multiple myeloma NA BeFree,GAD,LHGDN Detail
0.011 multiple sclerosis Association of methylenetetrahydrofolate reductase gene C677T polymorphism with ... BeFree,GAD 25203152 Detail
0.002 Muscle hypotonia NA GAD Detail
0.002 Muscle Spasticity NA GAD Detail
0.002 Musculoskeletal Diseases NA GAD Detail
0.002 Myeloproliferative disease NA GAD Detail
0.069 myocardial infarction NA BeFree,GAD,LHGDN Detail
0.002 Nasopharyngeal Neoplasms NA GAD Detail
0.003 Nausea NA BeFree,GAD Detail
0.120 Necrosis NA CTD_human Detail
0.123 Neoplasm Metastasis NA BeFree,CTD_human,GAD Detail
0.014 Neoplasm Recurrence, Local NA GAD Detail
0.002 nephrosclerosis NA GAD Detail
<0.001 nephrotic syndrome NA BeFree Detail
0.125 nervous system disorder NA BeFree,CTD_human,GAD Detail
0.222 Neural Tube Defects NA CTD_human,GAD,LHGDN Detail
0.127 neutropenia NA BeFree,CTD_human,GAD Detail
0.029 obesity The aim of the present study was to evaluate the effect of simvastatin treatment... BeFree,GAD 25115547 Detail
0.002 Obesity, Morbid NA GAD Detail
0.002 ocular hypertension NA GAD Detail
0.008 oligospermia NA BeFree,GAD Detail
0.017 Bone necrosis NA GAD,LHGDN Detail
0.014 Osteoporosis, Postmenopausal NA GAD Detail
0.008 osteosarcoma NA BeFree,GAD,LHGDN Detail
0.004 ovarian carcinoma NA BeFree Detail
<0.001 Ovarian Diseases NA BeFree Detail
<0.001 Pain Thus, we sought to determine the effects of polymorphisms in COMT and functional... BeFree 25218601 Detail
0.126 depressive disorder We found that genotype Met/Met of the Val66Met polymorphism of the brain-derived... BeFree 20163778 Detail
0.017 Pancreatic Neoplasm NA GAD,LHGDN Detail
0.002 pancreatitis NA GAD Detail
0.002 panuveitis NA GAD Detail
<0.001 papilloma NA BeFree Detail
0.016 Metabolic syndrome X We found that genotype Met/Met of the Val66Met polymorphism of the brain-derived... BeFree 20163778 Detail
0.002 periodontitis NA GAD Detail
0.121 Peripheral neuropathy NA BeFree,CTD_human Detail
0.005 Pharyngeal Neoplasms NA GAD Detail
0.002 Phenylketonurias NA GAD Detail
0.002 phlebitis NA GAD Detail
0.005 Placenta Disorders NA GAD Detail
0.002 Pleural Neoplasms NA GAD Detail
<0.001 pneumonia NA BeFree Detail
0.025 polycystic ovary syndrome NA BeFree,GAD,LHGDN Detail
0.002 polycythemia NA GAD Detail
<0.001 Adenomatous Polyposis Coli NA BeFree Detail
0.003 polyps NA BeFree,LHGDN Detail
0.028 Postoperative Complications NA GAD Detail
0.074 pre-eclampsia NA GAD,LHGDN Detail
0.005 Precancerous Conditions NA GAD Detail
0.009 Pregnancy Complications, Cardiovascular NA GAD Detail
0.028 Pregnancy Complications, Hematologic NA GAD Detail
0.003 Pregnancy in Diabetics NA BeFree,GAD Detail
0.009 Prenatal Exposure Delayed Effects NA GAD Detail
0.136 Prostatic Neoplasms NA CTD_human,GAD,LHGDN Detail
0.002 protein-energy malnutrition NA GAD Detail
0.002 proteinuria NA GAD Detail
0.008 psoriasis The Methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism is associated... BeFree,GAD 25449138 Detail
0.008 psoriasis Association between MTHFR 677C/T polymorphism and psoriasis risk: a meta-analysi... BeFree,GAD 25966157 Detail
0.002 Psychomotor Disorders NA GAD Detail
0.002 Psychoses, Substance-Induced NA GAD Detail
<0.001 Psychotic Disorders NA BeFree Detail
0.002 Puerperal Disorders NA GAD Detail
0.141 pulmonary embolism NA BeFree,CTD_human,GAD Detail
0.002 pulmonary fibrosis NA GAD Detail
0.002 pulmonary valve stenosis NA GAD Detail
0.003 Henoch-Schoenlein purpura NA BeFree,GAD Detail
0.002 Purpura, Thrombotic Thrombocytopenic NA GAD Detail
<0.001 quadriplegia NA BeFree Detail
0.020 Rectal Neoplasms NA BeFree,GAD,LHGDN Detail
0.002 renal artery obstruction NA GAD Detail
<0.001 Renal Artery Stenosis NA BeFree Detail
0.005 kidney failure NA BeFree Detail
0.239 Down syndrome In the present study, we determined polymorphisms of MTHFR A222V (677C &gt; T), ... BeFree 15889417 Detail
0.002 Respiratory Distress Syndrome, Adult NA GAD Detail
0.135 Kidney Diseases We analyzed 821 subjects with hypertensive nephrosclerosis from the longitudinal... BeFree 21613384 Detail
0.141 bipolar disorder We investigated the effect of polymorphic variants of c.1298A&gt;C (Glu429Ala) a... BeFree 18513846 Detail
0.054 Migraine Disorders By multivariate logistic stepwise regression analysis, type of migraine, regular... BeFree 22290307 Detail
0.006 Malignant tumor of cervix Employing PCR-RFLPs and HRM analyses, we examined the prevalence of BHMT Arg239G... BeFree 21349258 Detail
0.032 Malignant neoplasm of urinary bladder Association between MTHFR Ala222Val (rs1801133) polymorphism and bladder cancer ... BeFree 23649653 Detail
0.007 retinal artery occlusion NA BeFree,GAD Detail
0.101 Malignant neoplasm of breast Association of MTHFR Ala222Val (rs1801133) polymorphism and breast cancer suscep... BeFree 23217001 Detail
0.021 breast carcinoma Association of MTHFR Ala222Val (rs1801133) polymorphism and breast cancer suscep... BeFree 23217001 Detail
0.004 Carcinoma of bladder Association between MTHFR Ala222Val (rs1801133) polymorphism and bladder cancer ... BeFree 23649653 Detail
0.245 Cardiovascular Diseases Genetic variation in folate-mediated one-carbon metabolism, other than the well-... BeFree 22103680 Detail
0.008 Heart Diseases The polymorphism 677C&gt;T (NM_005957.4:c.665C&gt;T/p.Ala222Val, rs1801133:C&gt;... BeFree 24616178 Detail
0.010 cervix carcinoma Employing PCR-RFLPs and HRM analyses, we examined the prevalence of BHMT Arg239G... BeFree 21349258 Detail
0.002 Retinal Diseases NA BeFree Detail
0.005 retinal vascular occlusion NA GAD Detail
0.003 retinoblastoma NA BeFree,GAD Detail
0.002 Rhinitis, Allergic, Perennial NA GAD Detail
0.003 riboflavin deficiency NA BeFree,GAD Detail
0.219 schizophrenia Meta-analyses of blood homocysteine levels for gender and genetic association st... BeFree,CTD_human,GAD,LHGDN 24535549 Detail
0.219 schizophrenia Methylenetetrahydrofolate reductase (MTHFR) polymorphism susceptibility to schiz... BeFree,CTD_human,GAD,LHGDN 24938371 Detail
0.219 schizophrenia MTHFR gene polymorphism and age of onset of schizophrenia and bipolar disorder. BeFree,CTD_human,GAD,LHGDN 25101272 Detail
0.003 systemic scleroderma NA BeFree,GAD Detail
0.003 Seizures NA BeFree,GAD Detail
0.002 Sex Chromosome Aberrations NA GAD Detail
0.002 Septic Shock NA GAD Detail
<0.001 Sickle Cell Trait Recurrent cerebral venous thrombosis associated with heterozygote methylenetetra... BeFree 25074331 Detail
0.126 Sinus Thrombosis, Intracranial NA BeFree,CTD_human,GAD Detail
0.125 Dermatologic disorders NA CTD_human,GAD Detail
0.007 Skin Neoplasms NA GAD Detail
<0.001 smallpox NA BeFree Detail
<0.001 Spina Bifida Cystica NA BeFree Detail
0.120 Spinal Cord Diseases NA BeFree,CTD_human Detail
0.002 Splenomegaly NA GAD Detail
<0.001 ankylosing spondylitis The effect of IL-4 and MTHFR gene variants in ankylosing spondylitis. BeFree 25060515 Detail
0.226 Stomach Neoplasms NA BeFree,CTD_human,GAD,LHGDN Detail
0.003 stomatitis NA BeFree,GAD Detail
0.002 Subarachnoid Hemorrhage NA GAD Detail
0.002 Substance Withdrawal Syndrome NA GAD Detail
0.003 Takayasu Arteritis NA BeFree,LHGDN Detail
<0.001 Giant Cell Arteritis NA BeFree Detail
<0.001 Temporomandibular Joint Disorders To investigate the potential role of polymorphisms in matrix metalloproteinase-9... BeFree 26244436 Detail
<0.001 Temporomandibular Joint Dysfunction Syndrome GSTM1 alone and MTHFR polymorphisms did not show an association with TMD. BeFree 26244436 Detail
0.002 Thrombasthenia NA GAD Detail
0.005 thromboangiitis obliterans NA GAD Detail
0.127 thrombocytopenia NA CTD_human,GAD Detail
0.048 Thromboembolism Purpose of the conducted study was to establish the role of point mutations of p... BeFree,GAD 24632656 Detail
0.048 Thromboembolism Association between MTHFR C677T polymorphism and venous thromboembolism risk in ... BeFree,GAD 25149317 Detail
0.094 thrombosis NA GAD,LHGDN Detail
0.120 thyrotoxicosis NA BeFree,CTD_human Detail
<0.001 tonsillitis NA BeFree Detail
0.005 Trisomy NA BeFree,GAD Detail
0.006 Turner syndrome NA BeFree,GAD Detail
0.003 Unipolar Depression Low folate intake in the presence of the functional MTHFR 677 C > T (rs1801133) ... BeFree 24532086 Detail
0.003 Unipolar Depression MTHFR: Genetic variants, expression analysis and COMT interaction in major depre... BeFree 26021967 Detail
0.120 Adverse reaction to drug NA CTD_human Detail
<0.001 uremia NA BeFree Detail
0.002 Urologic Neoplasms NA GAD Detail
0.003 Varicosity NA BeFree,GAD Detail
0.155 Vascular Diseases Prevalence of variants in methylenetetrahydrofolate reductase and the severity o... BeFree,CTD_human,GAD 25304246 Detail
0.155 Vascular Diseases The Methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism is associated... BeFree,CTD_human,GAD 25449138 Detail
0.002 venous insufficiency NA GAD Detail
0.208 Venous Thrombosis NA CTD_human,GAD,LHGDN Detail
0.002 Virilism NA GAD Detail
0.019 Vitamin B 12 Deficiency NA BeFree,GAD Detail
0.005 Vitamin B Deficiency NA GAD Detail
<0.001 vitiligo NA BeFree Detail
0.003 von Willebrand Disease NA BeFree,GAD Detail
0.002 Weight Gain NA GAD Detail
0.057 Malignant neoplasm of lung Heterozygote carriers of SNPs in CYP1A2 1545T&gt;C, -164C&gt;A and -740T&gt;G; C... BeFree 17259654 Detail
0.007 Carcinoma of lung Heterozygote carriers of SNPs in CYP1A2 1545T&gt;C, -164C&gt;A and -740T&gt;G; C... BeFree 17259654 Detail
<0.001 Wheezing NA BeFree Detail
0.003 Cerebral Thrombosis NA BeFree,GAD Detail
0.005 Helicobacter Infections NA GAD Detail
0.008 B-Cell Lymphomas NA BeFree,GAD,LHGDN Detail
0.013 diffuse large B-cell lymphoma NA BeFree,GAD Detail
0.001 Lymphoma, Large-Cell, Follicular NA BeFree Detail
<0.001 Precursor cell lymphoblastic lymphoma NA BeFree Detail
0.007 T-Cell Lymphoma NA BeFree,GAD Detail
0.003 spina bifida occulta NA BeFree,GAD Detail
0.045 spina bifida NA BeFree,GAD,LHGDN Detail
<0.001 ovarian hyperstimulation syndrome NA BeFree Detail
0.023 Peripheral Vascular Diseases NA BeFree,GAD,LHGDN Detail
0.002 Bronchial Hyperreactivity NA GAD Detail
0.007 Central Nervous System Neoplasms NA BeFree,GAD Detail
0.003 bacterial vaginosis NA BeFree,GAD Detail
0.005 Neoplasms, Second Primary NA BeFree,GAD Detail
<0.001 Ovarian Failure, Premature NA BeFree Detail
0.013 antiphospholipid syndrome NA BeFree,GAD,LHGDN Detail
0.002 Arthritis, Reactive NA GAD Detail
0.003 essential hypertension NA BeFree Detail
<0.001 pyoderma gangrenosum NA BeFree Detail
0.005 acute leukemia NA BeFree,GAD Detail
0.002 alcoholic neuropathy NA GAD Detail
<0.001 Depressive Symptoms NA BeFree Detail
0.003 Depressive Syndrome NA BeFree,GAD Detail
<0.001 Idiopathic Membranous Glomerulonephritis NA BeFree Detail
0.005 cataract NA BeFree,GAD Detail
<0.001 Sicca Syndrome The prevalence of the Factor V Leiden (FVL; G1691A) mutation and the methylenete... BeFree 23869056 Detail
0.003 Pancreatitis, Chronic NA BeFree,LHGDN Detail
0.008 Left Ventricular Hypertrophy NA BeFree,GAD,LHGDN Detail
0.019 Deep Vein Thrombosis Purpose of the conducted study was to establish the role of point mutations of p... BeFree,GAD 24632657 Detail
0.019 Deep Vein Thrombosis PAI-1 4G/5G and MTHFR C677T polymorphisms increased the accuracy of two predicti... BeFree,GAD 24715181 Detail
<0.001 Small cell carcinoma of lung NA BeFree Detail
0.054 Migraine Disorders We propose that vitamin B intake, coupled with MTHFR and oestrogen receptor 1 po... BeFree,GAD,LHGDN 24040787 Detail
0.054 Migraine Disorders Data were analyzed for association with migraine and for interaction with the MT... BeFree,GAD,LHGDN 25039261 Detail
0.022 Premature Birth NA GAD,LHGDN Detail
<0.001 Oral Cavity Carcinoma NA BeFree Detail
0.005 Intracranial Hemorrhages NA GAD Detail
0.023 Myocardial Ischemia However, we cannot exclude a direct causal effect of MTHFR C677T genotype on IHD... BeFree,GAD 24458267 Detail
0.006 Arterial thrombosis NA BeFree,GAD Detail
0.002 Thrombosis of cerebral veins Recurrent cerebral venous thrombosis associated with heterozygote methylenetetra... BeFree 25074331 Detail
0.001 Deep thrombophlebitis NA BeFree Detail
0.004 esophageal carcinoma NA BeFree Detail
0.004 congenital heart disease Association analysis between MTHFR genetic polymorphisms and the risk of congeni... BeFree 24720776 Detail
0.004 congenital heart disease Association between MTHFR C677T polymorphism and congenital heart disease. A fam... BeFree 25256053 Detail
0.004 congenital heart disease Association between MTHFR polymorphisms and congenital heart disease: a meta-ana... BeFree 25472587 Detail
0.004 congenital heart disease The association of the MTHFR c.1625A>C genetic variant with the risk of congenit... BeFree 25494855 Detail
<0.001 Complete trisomy 18 syndrome NA BeFree Detail
0.002 hypoplastic left heart syndrome NA GAD Detail
0.003 low tension glaucoma NA BeFree,GAD Detail
0.002 Malignant neoplasm of mouth NA BeFree Detail
<0.001 Recurrent major depressive episodes NA BeFree Detail
0.014 migraine with aura In addition, these MTHFD1 polymorphisms did not appear to influence the risk of ... BeFree,GAD,LHGDN 25039261 Detail
0.014 migraine with aura A cohort of 141 adult females of Caucasian descent with MA was genotyped for the... BeFree,GAD,LHGDN 25598270 Detail
0.001 central retinal vein occlusion NA BeFree Detail
0.010 Optic Neuropathy, Ischemic NA GAD,LHGDN Detail
<0.001 Hearing Loss, Mixed Conductive-Sensorineural NA BeFree Detail
0.003 acute myocardial infarction NA BeFree Detail
<0.001 Old myocardial infarction NA BeFree Detail
<0.001 Disease of capillaries NA BeFree Detail
0.001 portal vein thrombosis Thrombophilic genetic factors PAI-1 4G-4G and MTHFR 677TT as risk factors of alc... BeFree 25987440 Detail
<0.001 Congenital anomaly of aortic arch NA BeFree Detail
0.002 Cleft palate with cleft lip NA BeFree Detail
0.002 adrenoleukodystrophy NA GAD Detail
0.002 iron deficiency anemia NA GAD Detail
0.126 Malnutrition Pathogenic predisposing avenues increasing the hypercoagulability in celiac dise... BeFree,CTD_human,GAD 25149392 Detail
<0.001 Angelman syndrome NA BeFree Detail
0.010 HELLP syndrome NA BeFree,GAD Detail
0.002 Right Ventricular Hypertrophy NA GAD Detail
0.002 Aneurysm, Ruptured NA GAD Detail
0.020 Aortic Aneurysm, Abdominal NA BeFree,GAD,LHGDN Detail
0.123 Microvascular Angina NA BeFree,CTD_human,GAD Detail
0.013 exfoliation syndrome NA BeFree,GAD,LHGDN Detail
0.006 Adenomatous Polyps NA BeFree,GAD Detail
<0.001 cholangiocarcinoma NA BeFree Detail
0.136 Cervical Intraepithelial Neoplasia MTHFR/p53 polymorphisms as genetic factors for cervical intraepithelial neoplasi... BeFree,CTD_human,GAD,LHGDN 24474455 Detail
0.136 Cervical Intraepithelial Neoplasia Studies in populations unexposed to folic acid (FA) fortification have demonstra... BeFree,CTD_human,GAD,LHGDN 25302494 Detail
0.002 Lip and oral cavity carcinoma NA BeFree Detail
0.002 Congenital defects NA BeFree Detail
<0.001 Diplegia NA BeFree Detail
<0.001 Lesion of brain NA BeFree Detail
0.002 Neurotoxicity Syndromes NA GAD Detail
<0.001 Disorder of vein NA BeFree Detail
<0.001 Malignant neoplasm of female breast NA BeFree Detail
0.002 pancreatic carcinoma NA BeFree Detail
<0.001 Bipolar II disorder A potential interaction between COMT and MTHFR genetic variants in Han Chinese p... BeFree 25744938 Detail
<0.001 Fibrosis, Liver NA BeFree Detail
<0.001 Thrombotic stroke NA BeFree Detail
0.005 coronary stenosis NA BeFree,GAD Detail
<0.001 Dyslipidemias The aim of the present study was to evaluate the effect of simvastatin treatment... BeFree 25115547 Detail
0.003 Erectile dysfunction NA BeFree,GAD Detail
0.057 Malignant neoplasm of lung Methylenetetrahydrofolate reductase 677TT genotype may be associated with an inc... BeFree,GAD 25544260 Detail
0.057 Malignant neoplasm of lung Allele and Genotype Frequencies of the Polymorphic Methylenetetrahydrofolate Red... BeFree,GAD 25921104 Detail
0.007 age related macular degeneration NA GAD Detail
0.002 Acute Lung Injury NA GAD Detail
0.002 Gonadal Dysgenesis, 45,X NA GAD Detail
<0.001 Neoplasm, Residual NA BeFree Detail
0.002 Oxidative Stress NA GAD Detail
0.002 Disease Progression NA GAD Detail
0.011 protein S deficiency NA BeFree,GAD Detail
0.002 multiple chemical sensitivity NA GAD Detail
0.002 Impotence, Vasculogenic NA GAD Detail
0.002 Sepsis NA GAD Detail
<0.001 Carcinoma, Small Cell NA BeFree Detail
<0.001 Childhood asthma NA BeFree Detail
<0.001 Renal sclerosis with hypertension NA BeFree Detail
0.002 gastroschisis NA GAD Detail
<0.001 Mesenteric Venous Thrombosis NA BeFree Detail
<0.001 Xeroderma Pigmentosum, Complementation Group D NA BeFree Detail
<0.001 Arakawa syndrome 2 NA BeFree Detail
0.003 5,10-Methylenetetrahydrofolate reductase deficiency NA BeFree Detail
0.120 Leukoencephalopathies NA CTD_human Detail
0.003 lateral sinus thrombosis NA BeFree,LHGDN Detail
0.003 essential tremor NA BeFree,GAD Detail
0.002 Impaired glucose tolerance NA GAD Detail
<0.001 Severe hereditary factor VIII deficiency disease NA BeFree Detail
0.003 antithrombin III deficiency NA BeFree,GAD Detail
0.002 Hemifacial Spasm NA GAD Detail
<0.001 Stage III Colon Cancer NA BeFree Detail
<0.001 Malignant neoplasm of colon stage IV NA BeFree Detail
<0.001 gastric adenocarcinoma NA BeFree Detail
<0.001 Non-small cell lung cancer metastatic NA BeFree Detail
0.004 Cancer of Head and Neck MTHFR C677T gene polymorphism and head and neck cancer risk: a meta-analysis bas... BeFree,GAD 25802478 Detail
0.004 Squamous cell carcinoma of esophagus NA BeFree Detail
0.001 Adenocarcinoma Of Esophagus In a Western European population the role of the MTHFR gene has not previously b... BeFree 25232254 Detail
0.003 Conventional (Clear Cell) Renal Cell Carcinoma NA BeFree,GAD Detail
<0.001 Solid tumour 5-Fluorouracil (5-FU), the mainstay of solid tumor chemotherapy over the past 40... BeFree 24434920 Detail
<0.001 Primary central nervous system lymphoma NA BeFree Detail
0.010 cervix carcinoma MTHFR/p53 polymorphisms as genetic factors for cervical intraepithelial neoplasi... BeFree,GAD 24474455 Detail
0.002 Lupus anticoagulant disorder NA BeFree Detail
0.122 Arsenic Poisoning NA CTD_human,GAD Detail
<0.001 Dryness of eye Also, it is determined an association between MTHFR C677T polymorphism and feeli... BeFree 25824380 Detail
<0.001 Anastomosis NA BeFree Detail
0.003 Restenosis NA BeFree,GAD Detail
0.125 Inflammatory disease of mucous membrane NA CTD_human,GAD Detail
0.005 Atrophic NA GAD,LHGDN Detail
<0.001 Squamous intraepithelial lesion NA BeFree Detail
0.006 Common Migraine NA BeFree,GAD Detail
<0.001 Non-arteritic ischemic optic neuropathy NA BeFree Detail
<0.001 Cerebral venous sinus thrombosis NA BeFree Detail
0.005 Vertebral Artery Dissection NA GAD Detail
0.003 Impaired cognition NA BeFree Detail
<0.001 Proliferative retinopathy NA BeFree Detail
<0.001 Venous retinal branch occlusion NA BeFree Detail
0.002 Glaucoma, Primary Open Angle Ours is the first report demonstrating association of MTHFR C677T with POAG but ... BeFree 25054348 Detail
0.004 Deep vein thrombosis of lower limb Purpose of the conducted study was to establish the role of point mutations of p... BeFree 24632657 Detail
0.004 Deep vein thrombosis of lower limb PAI-1 4G/5G and MTHFR C677T polymorphisms increased the accuracy of two predicti... BeFree 24715181 Detail
0.012 Complications of Diabetes Mellitus NA GAD Detail
<0.001 Lemierre Syndrome Lemierre's syndrome with double heterozygote status in the methylenetetrahydrofo... BeFree 24668238 Detail
<0.001 Double inlet left ventricle NA BeFree Detail
0.004 Malignant neoplasm of pancreas NA BeFree,GAD Detail
<0.001 Nonorganic psychosis NA BeFree Detail
<0.001 Cervical intraepithelial neoplasia grade 1 NA BeFree Detail
0.001 Cervical intraepithelial neoplasia grade 2 This study provides the first evidence that the MTHFR 677CT/TT genotype-associat... BeFree 25302494 Detail
<0.001 Helicobacter pylori (H. pylori) infection in conditions classified elsewhere and of unspecified site NA BeFree Detail
0.005 Avitaminosis NA BeFree,GAD Detail
<0.001 Diagnosis, Psychiatric NA BeFree Detail
0.030 Malignant neoplasm of prostate The protective effect of methylenetetrahydrofolate reductase C677T polymorphism ... BeFree,GAD 25841988 Detail
0.011 Hematologic Neoplasms NA BeFree,GAD,LHGDN Detail
0.216 thrombophilia Purpose of the conducted study was to establish the role of point mutations of p... BeFree,CTD_human,GAD,LHGDN 24632656 Detail
0.216 thrombophilia Purpose of the conducted study was to establish the role of point mutations of p... BeFree,CTD_human,GAD,LHGDN 24632657 Detail
0.216 thrombophilia A postmortem genetic testing for common mutations resulting in thrombophilia sho... BeFree,CTD_human,GAD,LHGDN 25074331 Detail
0.216 thrombophilia Pathogenic predisposing avenues increasing the hypercoagulability in celiac dise... BeFree,CTD_human,GAD,LHGDN 25149392 Detail
0.011 protein C deficiency Of the 58 patients, 30 had factor V Leiden mutation (5 homozygous, 25 heterozygo... BeFree,GAD 25326427 Detail
<0.001 Chronic Kidney Insufficiency NA BeFree Detail
<0.001 Chronic rejection of renal transplant NA BeFree Detail
<0.001 lupus erythematosus NA BeFree Detail
<0.001 Primary antiphospholipid syndrome NA BeFree Detail
<0.001 neuropathy NA BeFree Detail
0.002 Blind Vision NA GAD Detail
<0.001 endometrial carcinoma NA BeFree Detail
<0.001 Secondary malignant neoplasm of liver NA BeFree Detail
0.009 dementia NA BeFree,GAD Detail
0.002 body mass NA GAD Detail
0.003 Sleep Apnea, Obstructive NA BeFree,GAD Detail
<0.001 Pervasive Development Disorder NA BeFree Detail
0.003 Pulmonary Thromboembolisms NA BeFree,GAD Detail
0.002 Retinal Neoplasms NA GAD Detail
<0.001 Neurodegenerative Disorders NA BeFree Detail
0.011 Hepatitis C, Chronic NA BeFree,GAD,LHGDN Detail
0.120 Maxillofacial Abnormalities NA CTD_human Detail
<0.001 Mood Disorders NA BeFree Detail
0.042 Malignant neoplasm of esophagus NA BeFree,GAD Detail
<0.001 Palmar-plantar erythrodysesthesia syndrome NA BeFree Detail
0.001 Thyroid carcinoma Significant association between MTHFR C677T polymorphism and thyroid cancer risk... BeFree 25007377 Detail
0.001 Thyroid carcinoma The association between the C677T polymorphism in MTHFR gene and the risk of thy... BeFree 25070812 Detail
<0.001 Squamous cell carcinoma of skin NA BeFree Detail
0.245 Cardiovascular Diseases Some examples include the alanine-to-valine substitution at codon 222 (Ala222--&... BeFree 11916749 Detail
<0.001 Liver and Intrahepatic Biliary Tract Carcinoma Associations between MTHFR Ala222Val polymorphism and risks of hepatitis and hep... BeFree 24155211 Detail
0.026 Glaucoma, Open-Angle The effect of MTHFR ala222val polymorphism on open-angle glaucoma: a meta-analys... BeFree 25317717 Detail
0.009 glioblastoma The methylenetetrahydrofolate reductase (MTHFR) variant c.677C&gt;T (A222V) infl... BeFree 18497326 Detail
0.029 Ischemic stroke The folate-sensitive polymorphism methylenetetrahydrofolate reductase (MTHFR) c.... BeFree 16053469 Detail
0.003 Malignant neoplasm of liver Associations between MTHFR Ala222Val polymorphism and risks of hepatitis and hep... BeFree 24155211 Detail
0.155 Vascular Diseases The 5,10-methylenetetrahydrofolate reductase ( MTHFR ) gene 677C --&gt; T polymo... BeFree 15576298 Detail
0.003 5,10-Methylenetetrahydrofolate reductase deficiency In contrast, carriers of the variant allele for the MTHFR (A222V) polymorphism h... BeFree 17469025 Detail
0.015 Ischemic Cerebrovascular Accident Methylenetetrahydrofolate reductase gene A222V polymorphism and risk of ischemic... BeFree 15576298 Detail
<0.001 Anemia, Hemolytic Some examples include the alanine-to-valine substitution at codon 222 (Ala222--&... BeFree 11916749 Detail
0.015 Ischemic Cerebrovascular Accident The folate-sensitive polymorphism methylenetetrahydrofolate reductase (MTHFR) c.... BeFree 16053469 Detail
0.032 Malignant neoplasm of urinary bladder This meta-analysis showed the evidence that MTHFR Ala222Val polymorphism was not... BeFree 23773402 Detail
<0.001 hepatitis Associations between MTHFR Ala222Val polymorphism and risks of hepatitis and hep... BeFree 24155211 Detail
0.029 Ischemic stroke Methylenetetrahydrofolate reductase gene A222V polymorphism and risk of ischemic... BeFree 15576298 Detail
0.337 hyperhomocysteinemia Hyperhomocysteinemia due to Methylenetetrahydrofolate Reductase (MTHFR) gene, in... BeFree 21854603 Detail
0.013 Malignant neoplasm of ovary Genetic polymorphisms of methylenetetrahydrofolate reductase (MTHFR) gene Ala222... BeFree 24146277 Detail
0.004 Carcinoma of bladder This meta-analysis showed the evidence that MTHFR Ala222Val polymorphism was not... BeFree 23773402 Detail
0.069 myocardial infarction Multivariable logistic regression analysis with adjustment for age, sex, body ma... BeFree 16894468 Detail
0.146 Homocysteinemia Hyperhomocysteinemia due to Methylenetetrahydrofolate Reductase (MTHFR) gene, in... BeFree 21854603 Detail
0.257 Cerebrovascular accident The genotype distributions of PON1 Q192R and MTHFR A222V, which affect lipid and... BeFree 20615707 Detail
0.011 Lupus Erythematosus, Systemic However, MTHFR 677C &gt; T (A222V) and MTHFD1 1958G &gt; A (R653Q) allele and ge... BeFree 17664238 Detail
0.257 Cerebrovascular accident The folate-sensitive polymorphism methylenetetrahydrofolate reductase (MTHFR) c.... BeFree 16053469 Detail
<0.001 Glioblastoma multiforme The methylenetetrahydrofolate reductase (MTHFR) variant c.677C&gt;T (A222V) infl... BeFree 18497326 Detail
0.004 ovarian carcinoma Genetic polymorphisms of methylenetetrahydrofolate reductase (MTHFR) gene Ala222... BeFree 24146277 Detail
0.008 Hypercholesterolemia Multivariable logistic regression analysis with adjustment for age, sex, body ma... BeFree 16894468 Detail
<0.001 hepatitis A Associations between MTHFR Ala222Val polymorphism and risks of hepatitis and hep... BeFree 24155211 Detail
<0.001 Maternal hypertension NA BeFree Detail
0.012 Methotrexate poisoning NA GAD Detail
0.005 Carotid Atherosclerosis NA BeFree,GAD Detail
0.019 Factor V Leiden mutation The Prevalence of Factor V Leiden (G1691A) and Methylenetetrahydrofolate Reducta... BeFree 23869056 Detail
0.019 Factor V Leiden mutation The genetic polymorphisms for plasminogen activator inhibitor-1 4G/5G (PAI-1), F... BeFree 24484533 Detail
0.019 Factor V Leiden mutation Purpose of the conducted study was to establish the role of point mutations of p... BeFree 24632656 Detail
0.019 Factor V Leiden mutation Purpose of the conducted study was to establish the role of point mutations of p... BeFree 24632657 Detail
0.019 Factor V Leiden mutation Of the 58 patients, 30 had factor V Leiden mutation (5 homozygous, 25 heterozygo... BeFree 25326427 Detail
0.003 Alcohol Withdrawal Seizures NA BeFree,GAD Detail
<0.001 Severe depression NA BeFree Detail
<0.001 Carcinoma of larynx MTHFR 677TT (OR = 2.26, 95%CI = 1.09-4.87, P = 0.02) and T allele (OR = 1.40, 95... BeFree 25078601 Detail
<0.001 alcohol use disorder This study aimed to investigate the association of alcohol use disorder (AUD) wi... BeFree 19637400 Detail
0.014 Carcinogenesis The role of folic acid in carcinogenesis may be modulated by polymorphism C677T ... BeFree 25341694 Detail
<0.001 Leukemogenesis NA BeFree Detail
0.004 prostate carcinoma The protective effect of methylenetetrahydrofolate reductase C677T polymorphism ... BeFree 25841988 Detail
0.026 Activated Protein C Resistance NA BeFree,GAD Detail
0.002 hepatopulmonary syndrome NA GAD Detail
0.005 Choroidal Neovascularization NA GAD Detail
<0.001 Emotional problems NA BeFree Detail
0.002 Epithelial ovarian cancer NA GAD Detail
0.021 breast carcinoma Association of 677 C>T (rs1801133) and 1298 A>C (rs1801131) polymorphisms in the... BeFree 24945727 Detail
0.021 breast carcinoma A meta-analysis of genotypes and haplotypes of methylenetetrahydrofolate reducta... BeFree 24973876 Detail
0.021 breast carcinoma Association of dietary intake of folate and MTHFR genotype with breast cancer ri... BeFree 25078601 Detail
0.021 breast carcinoma The methylenetetrahydrofolate reductase C677T polymorphism and breast cancer ris... BeFree 25081713 Detail
0.021 breast carcinoma Association of methylenetetrahydrofolate reductase and methionine synthase polym... BeFree 25217320 Detail
0.021 breast carcinoma We found both a gene-environment (FGFR2-exercise activity) and a gene-gene (FGFR... BeFree 25270516 Detail
0.021 breast carcinoma Controversial roles of methylenetetrahydrofolate reductase polymorphisms and fol... BeFree 25318348 Detail
0.021 breast carcinoma Polymorphisms in the MTHFR gene are associated with breast cancer risk and progn... BeFree 25566964 Detail
0.021 breast carcinoma Breast cancer risk associated with gene expression and genotype polymorphisms of... BeFree 25801246 Detail
0.021 breast carcinoma Relationship of MTHFR and NQO1 Pharmacogenetics and Chemotherapy Clinical Outcom... BeFree 26014925 Detail
0.007 Carcinoma of lung Methylenetetrahydrofolate reductase 677TT genotype may be associated with an inc... BeFree 25544260 Detail
0.007 Carcinoma of lung Allele and Genotype Frequencies of the Polymorphic Methylenetetrahydrofolate Red... BeFree 25921104 Detail
<0.001 Hemophilia, NOS NA BeFree Detail
<0.001 Secondary malignant neoplasm of lymph node NA BeFree Detail
0.036 Pregnancy loss NA GAD Detail
0.005 Chronic progressive chorea NA GAD Detail
0.005 colon carcinoma 5,10-Methylenetetrahydrofolate reductase polymorphisms and colon cancer risk: a ... BeFree 25339013 Detail
0.004 Carcinoma of bladder NA BeFree Detail
0.003 skin carcinoma Genetic polymorphisms in genes encoding the prednisolone receptor, GST enzyme, M... BeFree,GAD 25616102 Detail
<0.001 Dissecting aneurysm of the thoracic aorta NA BeFree Detail
<0.001 Subfertility NA BeFree Detail
0.002 Microalbuminuria NA BeFree Detail
0.012 hyperuricemia NA BeFree,GAD,LHGDN Detail
0.003 Cardiac defects NA BeFree,GAD Detail
<0.001 cardiac event NA BeFree Detail
<0.001 End Stage Liver Disease NA BeFree Detail
0.003 early pregnancy NA BeFree Detail
0.001 vascular disease occlusive NA BeFree Detail
<0.001 Brain Tumor, Primary NA BeFree Detail
<0.001 Cystathionine beta-Synthase Deficiency Disease NA BeFree Detail
0.002 Subarachnoid Hemorrhage, Aneurysmal NA GAD Detail
0.002 CADASIL Syndrome NA GAD Detail
0.003 adult acute lymphocytic leukemia NA BeFree Detail
<0.001 anterior ischemic optic neuropathy NA BeFree Detail
0.005 Carotid Artery, Internal, Dissection NA GAD Detail
0.008 brain infarction NA BeFree,GAD Detail
0.005 Intracranial Arterial Diseases NA GAD Detail
0.009 intracranial thrombosis NA GAD Detail
0.002 Hypoxia-Ischemia, Brain NA GAD Detail
0.002 Embryo Loss NA GAD Detail
0.003 Congenital omphalocele NA BeFree,GAD Detail
0.003 Cleft lip with or without cleft palate rs1801133C>T polymorphism in MTHFR is a risk factor for nonsyndromic cleft lip w... BeFree 25808365 Detail
0.001 Helicobacter pylori infection Impact of methylenetetrahydrofolate reductase polymorphisms and folate intake on... BeFree 24615072 Detail
0.005 Pregnancy associated hypertension NA GAD Detail
0.132 Blood Coagulation Disorders, Inherited NA CTD_human,GAD Detail
<0.001 Sickle Cell Dactylitis NA BeFree Detail
0.002 Arteriopathic disease NA BeFree Detail
<0.001 Myelosuppression NA BeFree Detail
0.003 Endothelial dysfunction To confirm previous observations on the association of homozygosity for the TT M... BeFree 26137654 Detail
0.006 Budd-Chiari syndrome NA BeFree,GAD,LHGDN Detail
0.001 Acute GVH disease NA BeFree Detail
0.132 Drug-Induced Liver Injury NA CTD_human,GAD Detail
<0.001 Psychotic symptom NA BeFree Detail
0.003 Optic Atrophy, Hereditary, Leber NA BeFree,GAD Detail
0.239 Coronary heart disease Compound mutants for (MTHFD-G1958A, MTHFR-C677T and MTR-A2756G) and (MTHFD-G1958... BeFree 23701284 Detail
0.016 Acute lymphocytic leukemia We investigated preliminarily whether methylenetetrahydrofolate reductase (MTHFR... BeFree 18458567 Detail
<0.001 Cerebral Ischemia The methylenetetrahydrofolate reductase (MTHFR) 677C>T and 1298A>C polymorphisms... BeFree 25098357 Detail
<0.001 transient cerebral ischemia NA BeFree Detail
0.003 retinoblastoma A case-control study of 72 retinoblastoma cases and 98 cancer-free children cont... BeFree 20310006 Detail
0.029 obesity C677t polymorphism of MTHFR and G80A polymorphism of RFC genes and their relatio... BeFree 21681722 Detail
<0.001 Central neuroblastoma The aim of this study was to investigate the association between MTHFR rs1801133... BeFree 25536437 Detail
0.006 ovarian neoplasm NA BeFree,LHGDN Detail
0.337 hyperhomocysteinemia To the best of our knowledge, this is the first family with multiple AIS patient... BeFree 18958479 Detail
0.002 Genomic Instability NA GAD Detail
0.120 Microsatellite Instability NA CTD_human Detail
0.021 breast carcinoma Conversely, for women over 50, the risk of breast cancer development was statist... BeFree 22134752 Detail
0.146 Homocysteinemia To the best of our knowledge, this is the first family with multiple AIS patient... BeFree 18958479 Detail
0.003 Acute coronary syndrome NA BeFree,GAD Detail
0.005 Leukoaraiosis NA GAD,LHGDN Detail
0.232 Precursor Cell Lymphoblastic Leukemia Lymphoma Children with ALL (n = 96) were screened for GCPII C1561T, RFC1 G80A, cSHMT C142... BeFree 22838948 Detail
0.001 Colorectal cancer metastatic NA BeFree Detail
0.125 coronary restenosis NA CTD_human,GAD Detail
0.232 Precursor Cell Lymphoblastic Leukemia Lymphoma We investigated preliminarily whether methylenetetrahydrofolate reductase (MTHFR... BeFree 18458567 Detail
0.003 nephroblastoma The aim of this study was to investigate the association between MTHFR rs1801133... BeFree 25536437 Detail
0.007 Papillomavirus Infections NA GAD Detail
0.016 Acute lymphocytic leukemia Children with ALL (n = 96) were screened for GCPII C1561T, RFC1 G80A, cSHMT C142... BeFree 22838948 Detail
0.002 Macroangiopathy NA BeFree Detail
0.257 Cerebrovascular accident Two siblings with a homozygous MTHFR C677T (G80A-RFC1) mutation and stroke. BeFree 18958479 Detail
0.021 breast carcinoma Genetic polymorphisms of glutathione S-transferase (GST) genes including GSTT1 p... BeFree 17180579 Detail
0.013 Malignant neoplasm of ovary NA BeFree,GAD Detail
<0.001 Sporadic Breast Carcinoma Reduced folate carrier 1 (RFC1) G80A and methylenetetrahydrofolate reductase (MT... BeFree 21113649 Detail
0.101 Malignant neoplasm of breast Genetic polymorphisms of glutathione S-transferase (GST) genes including GSTT1 p... BeFree 17180579 Detail
0.101 Malignant neoplasm of breast Conversely, for women over 50, the risk of breast cancer development was statist... BeFree 22134752 Detail
<0.001 Skin toxicity NA BeFree Detail
<0.001 Precursor cell lymphoblastic lymphoma We investigated preliminarily whether methylenetetrahydrofolate reductase (MTHFR... BeFree 18458567 Detail
0.239 Down syndrome In conclusion, the presence of three or more polymorphic alleles for MTHFR C677T... BeFree 18273817 Detail
0.002 Squamous cell carcinoma of the head and neck NA BeFree Detail
<0.001 neuroblastoma The aim of this study was to investigate the association between MTHFR rs1801133... BeFree 25536437 Detail
0.003 prothrombin gene mutation NA BeFree Detail
0.002 Stenosis NA GAD Detail
0.003 sarcoma NA BeFree,LHGDN Detail
0.005 major depressive disorder Low folate intake in the presence of the functional MTHFR 677 C > T (rs1801133) ... BeFree,GAD 24532086 Detail
0.005 major depressive disorder MTHFR: Genetic variants, expression analysis and COMT interaction in major depre... BeFree,GAD 26021967 Detail
0.125 Blood pressure finding NA GAD,GWASCAT Detail
0.127 Systemic arterial pressure NA GAD,GWASCAT Detail
0.004 Adenoma of large intestine NA BeFree Detail
0.001 childhood leukemia The association of methylenetetrahydrofolate reductase genotypes with the risk o... BeFree 25793509 Detail
<0.001 gastric cardia adenocarcinoma NA BeFree Detail
0.002 gastric cardia carcinoma NA GAD Detail
<0.001 Hereditary Nonpolyposis Colorectal Cancer NA BeFree Detail
0.003 Infiltrating Cervical Carcinoma The MTHFR/p53 genetic combinations AA/ArgArg and AA/ArgPro are associated geneti... BeFree,GAD 24474455 Detail
0.002 Necrotic changes (finding) NA GAD Detail
<0.001 Sporadic Breast Carcinoma NA BeFree Detail
<0.001 differentiated thyroid gland carcinoma NA BeFree Detail
0.002 hearing impairment NA GAD Detail
<0.001 Avascular necrosis of the capital femoral epiphysis NA BeFree Detail
<0.001 Severe diarrhea NA BeFree Detail
<0.001 alpha^+^ Thalassemia NA BeFree Detail
0.161 Mammary Neoplasms NA CTD_human,GAD,LHGDN Detail
<0.001 Vitamin Deficiency NA BeFree Detail
0.001 Autism Spectrum Disorders NA BeFree Detail
<0.001 Rectal Tumors NA BeFree Detail
0.003 Thrombosis of retinal vein NA BeFree,GAD Detail
<0.001 Rash and Dermatitis Adverse Event Associated with Chemoradiation NA BeFree Detail
0.001 Chronic Kidney Diseases A total of 40 male patients with CKD and stable renal function (Kidney Disease O... BeFree 24711158 Detail
0.004 Renal Insufficiency NA BeFree,GAD Detail
<0.001 Oral Mucositis NA BeFree Detail
<0.001 Glioblastoma multiforme NA BeFree Detail
<0.001 Cirrhosis NA BeFree Detail
<0.001 Nephrotic Syndrome, Minimal Change NA BeFree Detail
0.002 Peripheral Arterial Diseases NA BeFree Detail
<0.001 Non-Neoplastic Disorder NA BeFree Detail
<0.001 Dysmorphism NA BeFree Detail
0.003 Fetus affected by placental transfer of anticonvulsant NA BeFree,GAD Detail
<0.001 Meningioma, benign, no ICD-O subtype NA BeFree Detail
<0.001 Fast acetylator due to N-acetyltransferase enzyme variant NA BeFree Detail
<0.001 Coronary heart disease, susceptibility to, 5 NA BeFree Detail
<0.001 TIBIAL MUSCULAR DYSTROPHY, TARDIVE GSTM1 alone and MTHFR polymorphisms did not show an association with TMD. BeFree 26244436 Detail
0.002 ASPIRIN RESISTANCE NA GAD Detail
<0.001 Azoospermia, Nonobstructive NA BeFree Detail
<0.001 VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding) NA BeFree Detail
<0.001 Nonarteritic anterior ischemic optic neuropathy (NAION) NA BeFree Detail
<0.001 Methylcobalamin Deficiency, CblG Type NA BeFree Detail
0.362 HOMOCYSTINURIA DUE TO DEFICIENCY OF N(5,10)-METHYLENETETRAHYDROFOLATE REDUCTASE ACTIVITY The diagnosis of MTHFR deficiency was confirmed based on extremely reduced fibro... BeFree,CLINVAR,ORPHANET,UNIPROT 25079578 Detail
0.123 Methylenetetrahydrofolate reductase deficiency NA BeFree,CTD_human,GAD Detail
0.002 THROMBOPHILIA DUE TO ACTIVATED PROTEIN C RESISTANCE (disorder) NA BeFree Detail
0.033 Venous thromboembolism NA GAD,LHGDN Detail
0.121 orofacial cleft 1 NA BeFree,CTD_human Detail
0.200 Neural tube defect, folate-sensitive NA CTD_human,MGD Detail
<0.001 uterine corpus cancer NA BeFree Detail
0.135 coronary artery disease Methylenetetrahydrofolate reductase C677T polymorphism is associated with increa... BeFree,GAD,LHGDN 26095803 Detail
0.002 Precursor T-Cell Lymphoblastic Leukemia-Lymphoma NA GAD Detail
0.002 Proteinuria Adverse Event NA GAD Detail
<0.001 malignant neoplasm of large intestine stage IV NA BeFree Detail
0.030 liver carcinoma NA BeFree,GAD,LHGDN Detail
<0.001 Infarction of spinal cord MTHFR mutation can be considered a risk factor for thrombotic SCI, but it is not... BeFree 25376315 Detail
0.002 Chronic kidney disease stage 5 NA BeFree Detail
0.003 Prothrombin G20210A mutation NA BeFree Detail
0.001 Thrombophilia, hereditary NA BeFree Detail
<0.001 Acquired thrombophilia NA BeFree Detail
0.120 Acute kidney injury NA CTD_human Detail
0.002 Congenital cardiac malformations NA GAD Detail
<0.001 Steatohepatitis NA BeFree Detail
0.002 Weight Gain Adverse Event NA GAD Detail
0.069 myocardial infarction Of the chosen polymorphisms, two (Leu125Val PECAM1 and A1/A2 FVII) are related t... BeFree 23274712 Detail
0.002 Infection of amniotic sac and membranes, unspecified, unspecified trimester, not applicable or unspecified NA GAD Detail
0.009 Chronic ulcerative colitis NA GAD Detail
0.002 Recurrent pregnancy loss NA GAD Detail
<0.001 Moyamoya disease 1 The roles of methylenetetrahydrofolate reductase 677C>T and 1298A>C polymorphism... BeFree 25098357 Detail
<0.001 Nasopharyngeal carcinoma NA BeFree Detail
0.005 Cerebral Hemorrhage NA GAD,LHGDN Detail
0.002 Deficiency of glucose-6-phosphate dehydrogenase NA GAD Detail
<0.001 Stage III Colon Cancer AJCC v7 NA BeFree Detail
<0.001 Nonalcoholic Steatohepatitis NA BeFree Detail
<0.001 Severe dementia NA BeFree Detail
0.005 Juvenile arthritis NA BeFree,GAD Detail
0.002 granulomatosis with polyangiitis NA GAD Detail
<0.001 Hypertensive end stage renal disease NA BeFree Detail
<0.001 Allergic disposition NA BeFree Detail
<0.001 Allergic sensitization NA BeFree Detail
0.007 Infection NA GAD,LHGDN Detail
<0.001 Pneumonitis NA BeFree Detail
0.003 intellectual disability NA LHGDN Detail
<0.001 juvenile rheumatoid arthritis NA BeFree Detail
0.014 Hyperhomocystinemia NA GAD Detail
<0.001 Experimental Organism Basal Cell Carcinoma NA BeFree Detail
<0.001 Lymphoblastic leukemia in children NA BeFree Detail
0.002 Hearing Loss NA GAD Detail
0.017 Congenital Abnormality NA BeFree,GAD,LHGDN Detail
0.038 Spontaneous abortion NA GAD,LHGDN Detail
0.048 Abortion, Habitual NA GAD,LHGDN Detail
0.032 Abruptio Placentae NA GAD,LHGDN Detail
<0.001 acute pancreatitis NA BeFree Detail
0.054 adenocarcinoma NA BeFree,GAD,LHGDN Detail
0.045 adenoma NA BeFree,GAD,LHGDN Detail
<0.001 Affective Disorders, Psychotic NA BeFree Detail
<0.001 Osteoporosis, Age-Related NA BeFree Detail
0.002 Albuminuria NA GAD Detail
<0.001 alcohol use disorder NA BeFree Detail
0.020 Alcoholic Intoxication, Chronic NA BeFree,GAD Detail
0.120 alopecia NA CTD_human Detail
0.003 alpha-Thalassemia NA BeFree,GAD Detail
0.190 Alzheimer's disease Association of MTHFR and PICALM polymorphisms with Alzheimer's disease. BeFree,CTD_human,GAD,LHGDN 25359311 Detail
0.190 Alzheimer's disease The MTHFR C677T polymorphism contributes to increased risk of Alzheimer's diseas... BeFree,CTD_human,GAD,LHGDN 25486592 Detail
0.003 amyotrophic lateral sclerosis NA BeFree,GAD Detail
0.126 anemia NA BeFree,CTD_human,GAD Detail
0.003 Cooley's anemia NA BeFree,GAD Detail
<0.001 Anemia, Hemolytic NA BeFree Detail
<0.001 Anemia, Megaloblastic NA BeFree Detail
0.025 Anemia, Sickle Cell The Prevalence of Factor V Leiden (G1691A) and Methylenetetrahydrofolate Reducta... BeFree,GAD 23869056 Detail
0.128 anencephaly NA BeFree,GAD,LHGDN,ORPHANET Detail
0.002 Aneuploidy NA GAD Detail
0.005 Aneurysm, Dissecting Hyperhomocysteinemia and methylenetetrahydrofolate reductase polymorphism in cer... BeFree,GAD 24903192 Detail
0.002 Anoxia NA GAD Detail
<0.001 Anxiety Disorders NA BeFree Detail
0.002 Aortic coarctation NA GAD Detail
0.003 aortic valve stenosis NA BeFree,GAD Detail
0.002 Apnea NA GAD Detail
0.011 Arterial Occlusive Diseases NA BeFree,GAD Detail
0.026 arteriosclerosis NA BeFree,GAD Detail
<0.001 Arteriovenous fistula NA BeFree Detail
0.003 arthritis NA LHGDN Detail
0.003 Arthritis, Psoriatic NA BeFree,GAD Detail
0.013 asthma Our study reveals one low-frequency missense mutation in the GRASP gene that is ... BeFree,GAD,LHGDN 25591454 Detail
0.059 atherosclerosis NA BeFree,GAD,LHGDN Detail
0.122 atrial fibrillation NA GAD,GWASCAT Detail
0.131 autistic disorder NA BeFree,CTD_human,GAD Detail
0.001 Autoimmune Diseases Genetic risk factors are known to contribute to the etiology of MS. Methylenetet... BeFree 25203152 Detail
0.009 azoospermia NA BeFree,GAD Detail
0.002 Mental disorders NA BeFree Detail
0.133 Bladder Neoplasm Patients with urinary bladder neoplasms who had been followed up for a 5-year pe... BeFree 17469025 Detail
0.016 Behcet Syndrome NA BeFree,GAD Detail
0.014 beta thalassemia The prevalence of the Factor V Leiden (FVL; G1691A) mutation and the methylenete... BeFree,GAD 23869056 Detail
0.002 Biliary Tract Neoplasm NA GAD Detail
0.141 bipolar disorder Methylenetetrahydrofolate reductase (MTHFR) polymorphism susceptibility to schiz... BeFree,CTD_human,GAD,LHGDN 24938371 Detail
0.141 bipolar disorder MTHFR gene polymorphism and age of onset of schizophrenia and bipolar disorder. BeFree,CTD_human,GAD,LHGDN 25101272 Detail
0.141 bipolar disorder Because dopaminergic disturbance is thought to be involved in the development of... BeFree,CTD_human,GAD,LHGDN 25744938 Detail
0.032 Malignant neoplasm of urinary bladder NA BeFree,GAD Detail
0.133 Bladder Neoplasm NA BeFree,CTD_human,GAD,LHGDN Detail
0.010 Blood Coagulation Disorders NA BeFree,GAD Detail
0.002 Blood Platelet Disorders NA GAD Detail
0.003 Bone Marrow Diseases NA BeFree,GAD Detail
0.002 Bone neoplasms NA GAD Detail
<0.001 borderline personality disorder We conclude that MTHFR polymorphism is associated with SZ and BPD among Asian, A... BeFree 24938371 Detail
<0.001 borderline personality disorder Because dopaminergic disturbance is thought to be involved in the development of... BeFree 25744938 Detail
0.002 Brain Damage, Chronic NA GAD Detail
0.002 Brain Diseases NA GAD Detail
0.010 Brain Neoplasms NA BeFree,GAD,LHGDN Detail
0.101 Malignant neoplasm of breast Association of 677 C>T (rs1801133) and 1298 A>C (rs1801131) polymorphisms in the... BeFree,GAD 24945727 Detail
0.101 Malignant neoplasm of breast A meta-analysis of genotypes and haplotypes of methylenetetrahydrofolate reducta... BeFree,GAD 24973876 Detail
0.101 Malignant neoplasm of breast Association of dietary intake of folate and MTHFR genotype with breast cancer ri... BeFree,GAD 25078601 Detail
0.101 Malignant neoplasm of breast The methylenetetrahydrofolate reductase C677T polymorphism and breast cancer ris... BeFree,GAD 25081713 Detail
0.101 Malignant neoplasm of breast Association of methylenetetrahydrofolate reductase and methionine synthase polym... BeFree,GAD 25217320 Detail
0.101 Malignant neoplasm of breast We found both a gene-environment (FGFR2-exercise activity) and a gene-gene (FGFR... BeFree,GAD 25270516 Detail
0.101 Malignant neoplasm of breast Controversial roles of methylenetetrahydrofolate reductase polymorphisms and fol... BeFree,GAD 25318348 Detail
0.101 Malignant neoplasm of breast Polymorphisms in the MTHFR gene are associated with breast cancer risk and progn... BeFree,GAD 25566964 Detail
0.101 Malignant neoplasm of breast Breast cancer risk associated with gene expression and genotype polymorphisms of... BeFree,GAD 25801246 Detail
0.101 Malignant neoplasm of breast Relationship of MTHFR and NQO1 Pharmacogenetics and Chemotherapy Clinical Outcom... BeFree,GAD 26014925 Detail
0.003 bronchopulmonary dysplasia We conclude that MTHFR polymorphism is associated with SZ and BPD among Asian, A... BeFree,GAD 24938371 Detail
0.003 bronchopulmonary dysplasia Because dopaminergic disturbance is thought to be involved in the development of... BeFree,GAD 25744938 Detail
0.005 Burkitt lymphoma NA GAD Detail
0.008 Malignant tumor of colon 5,10-Methylenetetrahydrofolate reductase polymorphisms and colon cancer risk: a ... BeFree,GAD 25339013 Detail
<0.001 Malignant neoplasm of endometrium NA BeFree Detail
<0.001 female breast carcinoma NA BeFree Detail
<0.001 Malignant neoplasm of larynx MTHFR 677TT (OR = 2.26, 95%CI = 1.09-4.87, P = 0.02) and T allele (OR = 1.40, 95... BeFree 25078601 Detail
0.003 Rectal Carcinoma NA BeFree Detail
<0.001 Malignant neoplasm of skin NA BeFree Detail
0.001 Malignant neoplasm of thyroid Significant association between MTHFR C677T polymorphism and thyroid cancer risk... BeFree 25007377 Detail
0.001 Malignant neoplasm of thyroid The association between the C677T polymorphism in MTHFR gene and the risk of thy... BeFree 25070812 Detail
0.005 Non-small cell lung carcinoma Heterozygote advantage of methylenetetrahydrofolate reductase polymorphisms on c... BeFree,GAD 25104092 Detail
<0.001 renal cell carcinoma NA BeFree Detail
Annotation

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The aim was to examine the association and effect modification by serum folate and vitamin B12 level... DisGeNET Detail
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Pathogenic predisposing avenues increasing the hypercoagulability in celiac disease are multiple: nu... DisGeNET Detail
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The methylenetetrahydrofolate reductase (MTHFR) 677C>T and 1298A>C polymorphisms, which are associat... DisGeNET Detail
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MTHFR/p53 polymorphisms as genetic factors for cervical intraepithelial neoplasia and cervical cance... DisGeNET Detail
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Methylenetetrahydrofolate reductase C677T polymorphism is associated with increased risk of coronary... DisGeNET Detail
These preliminary findings indicate that these two MTHFR genetic polymorphisms are related with the ... DisGeNET Detail
In the maternal analysis, the MTHFR C677T polymorphism was significantly associated with CHD risk (O... DisGeNET Detail
Our results support the MTHFR -677T allele as a susceptibility factor for CHD in the Asian maternal ... DisGeNET Detail
Results from this study indicate that the MTHFR c.1625A>C genetic variant influences the risk of CHD... DisGeNET Detail
Methylenetetrahydrofolate reductase C677T polymorphism is associated with increased risk of coronary... DisGeNET Detail
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Significance of dietary folate intake, homocysteine levels and MTHFR 677 C>T genotyping in South Afr... DisGeNET Detail
Genetic polymorphisms of methylenetetrahydrofolate reductase (MTHFR) gene and susceptibility to depr... DisGeNET Detail
Significance of dietary folate intake, homocysteine levels and MTHFR 677 C>T genotyping in South Afr... DisGeNET Detail
Genetic polymorphisms of methylenetetrahydrofolate reductase (MTHFR) gene and susceptibility to depr... DisGeNET Detail
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Genetic variants in ICAM1, PPARGC1A and MTHFR are potentially associated with different phenotypes o... DisGeNET Detail
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Meta-analysis of Methylenetetrahydrofolate reductase maternal gene in Down syndrome: increased susce... DisGeNET Detail
Maternal methylenetetrahydrofolate reductase C677T polymorphism and down syndrome risk: a meta-analy... DisGeNET Detail
The frequency of the MTHFR 677C allele in DS mothers (79.8%) was significantly higher than in contro... DisGeNET Detail
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Also, it is determined an association between MTHFR C677T polymorphism and feeling of stiffness and ... DisGeNET Detail
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The mechanisms may include the following pathways: [TGFB1 or TNFA]-[IL1B]-[pre-eclampsia]; [TNFA or ... DisGeNET Detail
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A difference in the methylation levels of methylenetetrahydrofolate reductase (MTHFR) amplicon was o... DisGeNET Detail
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Angiotensin converting enzyme and methylenetetrahydrofolate reductase gene variations in fibromyalgi... DisGeNET Detail
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The present investigation on MTHFR C677T and glaucoma reveals that the TT genotype and T allele of t... DisGeNET Detail
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Ours is the first report demonstrating association of MTHFR C677T with POAG but not PACG in individu... DisGeNET Detail
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Studies have reported that the MTHFR C677T polymorphism was associated with the development of struc... DisGeNET Detail
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In conclusion, thrombo and fibro-genetic mechanisms of PAI-1 4G-4G and MTHFR 677TT, could have a rol... DisGeNET Detail
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A significant association was observed between the MTHFR 677T allele and increased risk of MetS, hig... DisGeNET Detail
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Variants in methylenetetrahydrofolate reductase are common in the general population and in patients... DisGeNET Detail
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A total of 40 male patients with CKD and stable renal function (Kidney Disease Outcomes Quality Init... DisGeNET Detail
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All subjects were genotyped for 13 polymorphic variants in the genes of xenobiotics detoxification C... DisGeNET Detail
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These findings confirm that the MTHFR C677T polymorphism could be considered as a good marker of the... DisGeNET Detail
MTHFR (677 and 1298) genotype of children with ALL and healthy adult controls were done by the PCR-r... DisGeNET Detail
The association between methylenetetrahydrofolate reductase C677 > T polymorphisms and risk of pedia... DisGeNET Detail
Lack of association between polymorphisms in genes MTHFR and MDR1 with risk of childhood acute lymph... DisGeNET Detail
Moreover, significantly decreased susceptibility to ALL was observed for MTHFR TA (p=0.030) and RAD5... DisGeNET Detail
Our results indicated that the MTHFR C677T T allele was a protective biomarker for childhood ALL in ... DisGeNET Detail
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All subjects were genotyped for 13 polymorphic variants in the genes of xenobiotics detoxification C... DisGeNET Detail
Methylenetetrahydrofolate reductase gene polymorphisms contribute to acute myeloid leukemia and chro... DisGeNET Detail
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Methylenetetrahydrofolate reductase gene polymorphisms contribute to acute myeloid leukemia and chro... DisGeNET Detail
The methylenetetrahydrofolate reductase (MTHFR) 677 C>T polymorphism increases the risk of developin... DisGeNET Detail
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In conclusion, thrombo and fibro-genetic mechanisms of PAI-1 4G-4G and MTHFR 677TT, could have a rol... DisGeNET Detail
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Further SNPs associated with CRC risk included several previously reported to be associated with can... DisGeNET Detail
Further SNPs associated with CRC risk included several previously reported to be associated with can... DisGeNET Detail
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All subjects were genotyped for 13 polymorphic variants in the genes of xenobiotics detoxification C... DisGeNET Detail
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SNPs in MTRR (rs13162612; OR = 0.25; 95% CI: 0.11-0.58; rs10512948; OR = 0.61; 95% CI: 0.41-0.90; rs... DisGeNET Detail
SNPs in MTRR (rs13162612; OR = 0.25; 95% CI: 0.11-0.58; rs10512948; OR = 0.61; 95% CI: 0.41-0.90; rs... DisGeNET Detail
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The roles of methylenetetrahydrofolate reductase 677C>T and 1298A>C polymorphisms in moyamoya diseas... DisGeNET Detail
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Association of methylenetetrahydrofolate reductase gene C677T polymorphism with multiple sclerosis i... DisGeNET Detail
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The aim of the present study was to evaluate the effect of simvastatin treatment on circulating Hcy ... DisGeNET Detail
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Thus, we sought to determine the effects of polymorphisms in COMT and functionally related pain gene... DisGeNET Detail
We found that genotype Met/Met of the Val66Met polymorphism of the brain-derived neurotrophic factor... DisGeNET Detail
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We found that genotype Met/Met of the Val66Met polymorphism of the brain-derived neurotrophic factor... DisGeNET Detail
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The Methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism is associated with various diseas... DisGeNET Detail
Association between MTHFR 677C/T polymorphism and psoriasis risk: a meta-analysis. DisGeNET Detail
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In the present study, we determined polymorphisms of MTHFR A222V (677C &gt; T), MTHFR E429A (1298A &... DisGeNET Detail
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We analyzed 821 subjects with hypertensive nephrosclerosis from the longitudinal National Institute ... DisGeNET Detail
We investigated the effect of polymorphic variants of c.1298A&gt;C (Glu429Ala) and c.677C&gt;T (Ala2... DisGeNET Detail
By multivariate logistic stepwise regression analysis, type of migraine, regular and sufficient diet... DisGeNET Detail
Employing PCR-RFLPs and HRM analyses, we examined the prevalence of BHMT Arg239Gln (rs3733890), MTR ... DisGeNET Detail
Association between MTHFR Ala222Val (rs1801133) polymorphism and bladder cancer susceptibility: a sy... DisGeNET Detail
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Association of MTHFR Ala222Val (rs1801133) polymorphism and breast cancer susceptibility: An update ... DisGeNET Detail
Association of MTHFR Ala222Val (rs1801133) polymorphism and breast cancer susceptibility: An update ... DisGeNET Detail
Association between MTHFR Ala222Val (rs1801133) polymorphism and bladder cancer susceptibility: a sy... DisGeNET Detail
Genetic variation in folate-mediated one-carbon metabolism, other than the well-known effects of the... DisGeNET Detail
The polymorphism 677C&gt;T (NM_005957.4:c.665C&gt;T/p.Ala222Val, rs1801133:C&gt;T) in methylenetetra... DisGeNET Detail
Employing PCR-RFLPs and HRM analyses, we examined the prevalence of BHMT Arg239Gln (rs3733890), MTR ... DisGeNET Detail
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Meta-analyses of blood homocysteine levels for gender and genetic association studies of the MTHFR C... DisGeNET Detail
Methylenetetrahydrofolate reductase (MTHFR) polymorphism susceptibility to schizophrenia and bipolar... DisGeNET Detail
MTHFR gene polymorphism and age of onset of schizophrenia and bipolar disorder. DisGeNET Detail
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Recurrent cerebral venous thrombosis associated with heterozygote methylenetetrahydrofolate reductas... DisGeNET Detail
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The effect of IL-4 and MTHFR gene variants in ankylosing spondylitis. DisGeNET Detail
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To investigate the potential role of polymorphisms in matrix metalloproteinase-9 (MMP-9), glutathion... DisGeNET Detail
GSTM1 alone and MTHFR polymorphisms did not show an association with TMD. DisGeNET Detail
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Purpose of the conducted study was to establish the role of point mutations of prothrombin (PGM) - 2... DisGeNET Detail
Association between MTHFR C677T polymorphism and venous thromboembolism risk in the Chinese populati... DisGeNET Detail
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Low folate intake in the presence of the functional MTHFR 677 C > T (rs1801133) polymorphism is an i... DisGeNET Detail
MTHFR: Genetic variants, expression analysis and COMT interaction in major depressive disorder. DisGeNET Detail
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Prevalence of variants in methylenetetrahydrofolate reductase and the severity of pulmonary vascular... DisGeNET Detail
The Methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism is associated with various diseas... DisGeNET Detail
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Heterozygote carriers of SNPs in CYP1A2 1545T&gt;C, -164C&gt;A and -740T&gt;G; CYP2A6 -47A&gt;C; MDR... DisGeNET Detail
Heterozygote carriers of SNPs in CYP1A2 1545T&gt;C, -164C&gt;A and -740T&gt;G; CYP2A6 -47A&gt;C; MDR... DisGeNET Detail
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The prevalence of the Factor V Leiden (FVL; G1691A) mutation and the methylenetetrahydrofolate reduc... DisGeNET Detail
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Purpose of the conducted study was to establish the role of point mutations of prothrombin (PHG) - 2... DisGeNET Detail
PAI-1 4G/5G and MTHFR C677T polymorphisms increased the accuracy of two prediction scores for the ri... DisGeNET Detail
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We propose that vitamin B intake, coupled with MTHFR and oestrogen receptor 1 polymorphisms, causes ... DisGeNET Detail
Data were analyzed for association with migraine and for interaction with the MTHFR C667T polymorphi... DisGeNET Detail
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However, we cannot exclude a direct causal effect of MTHFR C677T genotype on IHD. DisGeNET Detail
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Recurrent cerebral venous thrombosis associated with heterozygote methylenetetrahydrofolate reductas... DisGeNET Detail
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Association analysis between MTHFR genetic polymorphisms and the risk of congenital heart diseases i... DisGeNET Detail
Association between MTHFR C677T polymorphism and congenital heart disease. A family-based meta-analy... DisGeNET Detail
Association between MTHFR polymorphisms and congenital heart disease: a meta-analysis based on 9,329... DisGeNET Detail
The association of the MTHFR c.1625A>C genetic variant with the risk of congenital heart diseases in... DisGeNET Detail
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In addition, these MTHFD1 polymorphisms did not appear to influence the risk of MA conferred by the ... DisGeNET Detail
A cohort of 141 adult females of Caucasian descent with MA was genotyped for the MTHFR C677T variant... DisGeNET Detail
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Thrombophilic genetic factors PAI-1 4G-4G and MTHFR 677TT as risk factors of alcohol, cryptogenic li... DisGeNET Detail
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Pathogenic predisposing avenues increasing the hypercoagulability in celiac disease are multiple: nu... DisGeNET Detail
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MTHFR/p53 polymorphisms as genetic factors for cervical intraepithelial neoplasia and cervical cance... DisGeNET Detail
Studies in populations unexposed to folic acid (FA) fortification have demonstrated that MTHFR C677T... DisGeNET Detail
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A potential interaction between COMT and MTHFR genetic variants in Han Chinese patients with bipolar... DisGeNET Detail
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The aim of the present study was to evaluate the effect of simvastatin treatment on circulating Hcy ... DisGeNET Detail
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Methylenetetrahydrofolate reductase 677TT genotype may be associated with an increased lung cancer r... DisGeNET Detail
Allele and Genotype Frequencies of the Polymorphic Methylenetetrahydrofolate Reductase and Lung Canc... DisGeNET Detail
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MTHFR C677T gene polymorphism and head and neck cancer risk: a meta-analysis based on 23 publication... DisGeNET Detail
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In a Western European population the role of the MTHFR gene has not previously been investigated in ... DisGeNET Detail
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5-Fluorouracil (5-FU), the mainstay of solid tumor chemotherapy over the past 40 years, induces grad... DisGeNET Detail
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MTHFR/p53 polymorphisms as genetic factors for cervical intraepithelial neoplasia and cervical cance... DisGeNET Detail
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Also, it is determined an association between MTHFR C677T polymorphism and feeling of stiffness and ... DisGeNET Detail
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Ours is the first report demonstrating association of MTHFR C677T with POAG but not PACG in individu... DisGeNET Detail
Purpose of the conducted study was to establish the role of point mutations of prothrombin (PHG) - 2... DisGeNET Detail
PAI-1 4G/5G and MTHFR C677T polymorphisms increased the accuracy of two prediction scores for the ri... DisGeNET Detail
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Lemierre's syndrome with double heterozygote status in the methylenetetrahydrofolate reductase gene. DisGeNET Detail
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This study provides the first evidence that the MTHFR 677CT/TT genotype-associated lower degree of P... DisGeNET Detail
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The protective effect of methylenetetrahydrofolate reductase C677T polymorphism against prostate can... DisGeNET Detail
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Purpose of the conducted study was to establish the role of point mutations of prothrombin (PGM) - 2... DisGeNET Detail
Purpose of the conducted study was to establish the role of point mutations of prothrombin (PHG) - 2... DisGeNET Detail
A postmortem genetic testing for common mutations resulting in thrombophilia should be performed in ... DisGeNET Detail
Pathogenic predisposing avenues increasing the hypercoagulability in celiac disease are multiple: nu... DisGeNET Detail
Of the 58 patients, 30 had factor V Leiden mutation (5 homozygous, 25 heterozygous), 16 had prothrom... DisGeNET Detail
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Significant association between MTHFR C677T polymorphism and thyroid cancer risk: evidence from a me... DisGeNET Detail
The association between the C677T polymorphism in MTHFR gene and the risk of thyroid cancer: a meta-... DisGeNET Detail
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Some examples include the alanine-to-valine substitution at codon 222 (Ala222--&gt;Val) [DNA: C-to-T... DisGeNET Detail
Associations between MTHFR Ala222Val polymorphism and risks of hepatitis and hepatitis-related liver... DisGeNET Detail
The effect of MTHFR ala222val polymorphism on open-angle glaucoma: a meta-analysis. DisGeNET Detail
The methylenetetrahydrofolate reductase (MTHFR) variant c.677C&gt;T (A222V) influences overall survi... DisGeNET Detail
The folate-sensitive polymorphism methylenetetrahydrofolate reductase (MTHFR) c. 677 C &gt; T (A222V... DisGeNET Detail
Associations between MTHFR Ala222Val polymorphism and risks of hepatitis and hepatitis-related liver... DisGeNET Detail
The 5,10-methylenetetrahydrofolate reductase ( MTHFR ) gene 677C --&gt; T polymorphism causes an A22... DisGeNET Detail
In contrast, carriers of the variant allele for the MTHFR (A222V) polymorphism had significantly lon... DisGeNET Detail
Methylenetetrahydrofolate reductase gene A222V polymorphism and risk of ischemic stroke. DisGeNET Detail
Some examples include the alanine-to-valine substitution at codon 222 (Ala222--&gt;Val) [DNA: C-to-T... DisGeNET Detail
The folate-sensitive polymorphism methylenetetrahydrofolate reductase (MTHFR) c. 677 C &gt; T (A222V... DisGeNET Detail
This meta-analysis showed the evidence that MTHFR Ala222Val polymorphism was not contributed to the ... DisGeNET Detail
Associations between MTHFR Ala222Val polymorphism and risks of hepatitis and hepatitis-related liver... DisGeNET Detail
Methylenetetrahydrofolate reductase gene A222V polymorphism and risk of ischemic stroke. DisGeNET Detail
Hyperhomocysteinemia due to Methylenetetrahydrofolate Reductase (MTHFR) gene, in particular the C677... DisGeNET Detail
Genetic polymorphisms of methylenetetrahydrofolate reductase (MTHFR) gene Ala222Val and susceptibili... DisGeNET Detail
This meta-analysis showed the evidence that MTHFR Ala222Val polymorphism was not contributed to the ... DisGeNET Detail
Multivariable logistic regression analysis with adjustment for age, sex, body mass index, and the pr... DisGeNET Detail
Hyperhomocysteinemia due to Methylenetetrahydrofolate Reductase (MTHFR) gene, in particular the C677... DisGeNET Detail
The genotype distributions of PON1 Q192R and MTHFR A222V, which affect lipid and homocysteine metabo... DisGeNET Detail
However, MTHFR 677C &gt; T (A222V) and MTHFD1 1958G &gt; A (R653Q) allele and genotype frequencies d... DisGeNET Detail
The folate-sensitive polymorphism methylenetetrahydrofolate reductase (MTHFR) c. 677 C &gt; T (A222V... DisGeNET Detail
The methylenetetrahydrofolate reductase (MTHFR) variant c.677C&gt;T (A222V) influences overall survi... DisGeNET Detail
Genetic polymorphisms of methylenetetrahydrofolate reductase (MTHFR) gene Ala222Val and susceptibili... DisGeNET Detail
Multivariable logistic regression analysis with adjustment for age, sex, body mass index, and the pr... DisGeNET Detail
Associations between MTHFR Ala222Val polymorphism and risks of hepatitis and hepatitis-related liver... DisGeNET Detail
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The Prevalence of Factor V Leiden (G1691A) and Methylenetetrahydrofolate Reductase C677T Mutations i... DisGeNET Detail
The genetic polymorphisms for plasminogen activator inhibitor-1 4G/5G (PAI-1), Factor V Leiden (FVL)... DisGeNET Detail
Purpose of the conducted study was to establish the role of point mutations of prothrombin (PGM) - 2... DisGeNET Detail
Purpose of the conducted study was to establish the role of point mutations of prothrombin (PHG) - 2... DisGeNET Detail
Of the 58 patients, 30 had factor V Leiden mutation (5 homozygous, 25 heterozygous), 16 had prothrom... DisGeNET Detail
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MTHFR 677TT (OR = 2.26, 95%CI = 1.09-4.87, P = 0.02) and T allele (OR = 1.40, 95%CI = 1.03-1.90, P =... DisGeNET Detail
This study aimed to investigate the association of alcohol use disorder (AUD) with four candidate ge... DisGeNET Detail
The role of folic acid in carcinogenesis may be modulated by polymorphism C677T in MTHFR and tandem ... DisGeNET Detail
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The protective effect of methylenetetrahydrofolate reductase C677T polymorphism against prostate can... DisGeNET Detail
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Association of 677 C>T (rs1801133) and 1298 A>C (rs1801131) polymorphisms in the MTHFR gene and brea... DisGeNET Detail
A meta-analysis of genotypes and haplotypes of methylenetetrahydrofolate reductase gene polymorphism... DisGeNET Detail
Association of dietary intake of folate and MTHFR genotype with breast cancer risk. DisGeNET Detail
The methylenetetrahydrofolate reductase C677T polymorphism and breast cancer risk in Asian populatio... DisGeNET Detail
Association of methylenetetrahydrofolate reductase and methionine synthase polymorphisms with breast... DisGeNET Detail
We found both a gene-environment (FGFR2-exercise activity) and a gene-gene (FGFR2-MTHFR) interaction... DisGeNET Detail
Controversial roles of methylenetetrahydrofolate reductase polymorphisms and folate in breast cancer... DisGeNET Detail
Polymorphisms in the MTHFR gene are associated with breast cancer risk and prognosis in a Chinese po... DisGeNET Detail
Breast cancer risk associated with gene expression and genotype polymorphisms of the folate-metaboli... DisGeNET Detail
Relationship of MTHFR and NQO1 Pharmacogenetics and Chemotherapy Clinical Outcomes in Breast Cancer ... DisGeNET Detail
Methylenetetrahydrofolate reductase 677TT genotype may be associated with an increased lung cancer r... DisGeNET Detail
Allele and Genotype Frequencies of the Polymorphic Methylenetetrahydrofolate Reductase and Lung Canc... DisGeNET Detail
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5,10-Methylenetetrahydrofolate reductase polymorphisms and colon cancer risk: a meta-analysis. DisGeNET Detail
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Genetic polymorphisms in genes encoding the prednisolone receptor, GST enzyme, MC1R, MTHFR enzyme an... DisGeNET Detail
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rs1801133C>T polymorphism in MTHFR is a risk factor for nonsyndromic cleft lip with or without cleft... DisGeNET Detail
Impact of methylenetetrahydrofolate reductase polymorphisms and folate intake on the risk of gastric... DisGeNET Detail
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To confirm previous observations on the association of homozygosity for the TT MTHFR genotype with B... DisGeNET Detail
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Compound mutants for (MTHFD-G1958A, MTHFR-C677T and MTR-A2756G) and (MTHFD-G1958A, RFC1-G80A and MTR... DisGeNET Detail
We investigated preliminarily whether methylenetetrahydrofolate reductase (MTHFR) 677C/T or reduced ... DisGeNET Detail
The methylenetetrahydrofolate reductase (MTHFR) 677C>T and 1298A>C polymorphisms, which are associat... DisGeNET Detail
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A case-control study of 72 retinoblastoma cases and 98 cancer-free children controls was performed t... DisGeNET Detail
C677t polymorphism of MTHFR and G80A polymorphism of RFC genes and their relation with homocysteine ... DisGeNET Detail
The aim of this study was to investigate the association between MTHFR rs1801133 (C677T) and RFC-1 r... DisGeNET Detail
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To the best of our knowledge, this is the first family with multiple AIS patients harboring homozygo... DisGeNET Detail
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Conversely, for women over 50, the risk of breast cancer development was statistically associated wi... DisGeNET Detail
To the best of our knowledge, this is the first family with multiple AIS patients harboring homozygo... DisGeNET Detail
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Children with ALL (n = 96) were screened for GCPII C1561T, RFC1 G80A, cSHMT C1420T, TYMS 5´-UTR 2R3R... DisGeNET Detail
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We investigated preliminarily whether methylenetetrahydrofolate reductase (MTHFR) 677C/T or reduced ... DisGeNET Detail
The aim of this study was to investigate the association between MTHFR rs1801133 (C677T) and RFC-1 r... DisGeNET Detail
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Children with ALL (n = 96) were screened for GCPII C1561T, RFC1 G80A, cSHMT C1420T, TYMS 5´-UTR 2R3R... DisGeNET Detail
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Two siblings with a homozygous MTHFR C677T (G80A-RFC1) mutation and stroke. DisGeNET Detail
Genetic polymorphisms of glutathione S-transferase (GST) genes including GSTT1 positive/null, GSTM1 ... DisGeNET Detail
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Reduced folate carrier 1 (RFC1) G80A and methylenetetrahydrofolate reductase (MTHFR) C677T were asso... DisGeNET Detail
Genetic polymorphisms of glutathione S-transferase (GST) genes including GSTT1 positive/null, GSTM1 ... DisGeNET Detail
Conversely, for women over 50, the risk of breast cancer development was statistically associated wi... DisGeNET Detail
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We investigated preliminarily whether methylenetetrahydrofolate reductase (MTHFR) 677C/T or reduced ... DisGeNET Detail
In conclusion, the presence of three or more polymorphic alleles for MTHFR C677T, MTHFR A1298C, MTR ... DisGeNET Detail
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The aim of this study was to investigate the association between MTHFR rs1801133 (C677T) and RFC-1 r... DisGeNET Detail
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Low folate intake in the presence of the functional MTHFR 677 C > T (rs1801133) polymorphism is an i... DisGeNET Detail
MTHFR: Genetic variants, expression analysis and COMT interaction in major depressive disorder. DisGeNET Detail
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The association of methylenetetrahydrofolate reductase genotypes with the risk of childhood leukemia... DisGeNET Detail
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The MTHFR/p53 genetic combinations AA/ArgArg and AA/ArgPro are associated genetic risk factors for I... DisGeNET Detail
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A total of 40 male patients with CKD and stable renal function (Kidney Disease Outcomes Quality Init... DisGeNET Detail
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GSTM1 alone and MTHFR polymorphisms did not show an association with TMD. DisGeNET Detail
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The diagnosis of MTHFR deficiency was confirmed based on extremely reduced fibroblast MTHFR activity... DisGeNET Detail
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Methylenetetrahydrofolate reductase C677T polymorphism is associated with increased risk of coronary... DisGeNET Detail
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MTHFR mutation can be considered a risk factor for thrombotic SCI, but it is not the sole risk facto... DisGeNET Detail
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Of the chosen polymorphisms, two (Leu125Val PECAM1 and A1/A2 FVII) are related to myocardial infarct... DisGeNET Detail
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The roles of methylenetetrahydrofolate reductase 677C>T and 1298A>C polymorphisms in moyamoya diseas... DisGeNET Detail
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Association of MTHFR and PICALM polymorphisms with Alzheimer's disease. DisGeNET Detail
The MTHFR C677T polymorphism contributes to increased risk of Alzheimer's disease: evidence based on... DisGeNET Detail
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The Prevalence of Factor V Leiden (G1691A) and Methylenetetrahydrofolate Reductase C677T Mutations i... DisGeNET Detail
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Hyperhomocysteinemia and methylenetetrahydrofolate reductase polymorphism in cervical artery dissect... DisGeNET Detail
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Our study reveals one low-frequency missense mutation in the GRASP gene that is associated with asth... DisGeNET Detail
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Genetic risk factors are known to contribute to the etiology of MS. Methylenetetrahydrofolate reduct... DisGeNET Detail
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Patients with urinary bladder neoplasms who had been followed up for a 5-year period were genotyped ... DisGeNET Detail
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The prevalence of the Factor V Leiden (FVL; G1691A) mutation and the methylenetetrahydrofolate reduc... DisGeNET Detail
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Methylenetetrahydrofolate reductase (MTHFR) polymorphism susceptibility to schizophrenia and bipolar... DisGeNET Detail
MTHFR gene polymorphism and age of onset of schizophrenia and bipolar disorder. DisGeNET Detail
Because dopaminergic disturbance is thought to be involved in the development of bipolar disorder (B... DisGeNET Detail
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We conclude that MTHFR polymorphism is associated with SZ and BPD among Asian, African populations, ... DisGeNET Detail
Because dopaminergic disturbance is thought to be involved in the development of bipolar disorder (B... DisGeNET Detail
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Association of 677 C>T (rs1801133) and 1298 A>C (rs1801131) polymorphisms in the MTHFR gene and brea... DisGeNET Detail
A meta-analysis of genotypes and haplotypes of methylenetetrahydrofolate reductase gene polymorphism... DisGeNET Detail
Association of dietary intake of folate and MTHFR genotype with breast cancer risk. DisGeNET Detail
The methylenetetrahydrofolate reductase C677T polymorphism and breast cancer risk in Asian populatio... DisGeNET Detail
Association of methylenetetrahydrofolate reductase and methionine synthase polymorphisms with breast... DisGeNET Detail
We found both a gene-environment (FGFR2-exercise activity) and a gene-gene (FGFR2-MTHFR) interaction... DisGeNET Detail
Controversial roles of methylenetetrahydrofolate reductase polymorphisms and folate in breast cancer... DisGeNET Detail
Polymorphisms in the MTHFR gene are associated with breast cancer risk and prognosis in a Chinese po... DisGeNET Detail
Breast cancer risk associated with gene expression and genotype polymorphisms of the folate-metaboli... DisGeNET Detail
Relationship of MTHFR and NQO1 Pharmacogenetics and Chemotherapy Clinical Outcomes in Breast Cancer ... DisGeNET Detail
We conclude that MTHFR polymorphism is associated with SZ and BPD among Asian, African populations, ... DisGeNET Detail
Because dopaminergic disturbance is thought to be involved in the development of bipolar disorder (B... DisGeNET Detail
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5,10-Methylenetetrahydrofolate reductase polymorphisms and colon cancer risk: a meta-analysis. DisGeNET Detail
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MTHFR 677TT (OR = 2.26, 95%CI = 1.09-4.87, P = 0.02) and T allele (OR = 1.40, 95%CI = 1.03-1.90, P =... DisGeNET Detail
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Significant association between MTHFR C677T polymorphism and thyroid cancer risk: evidence from a me... DisGeNET Detail
The association between the C677T polymorphism in MTHFR gene and the risk of thyroid cancer: a meta-... DisGeNET Detail
Heterozygote advantage of methylenetetrahydrofolate reductase polymorphisms on clinical outcomes in ... DisGeNET Detail
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Gene
-
dbSNP
rs386514057 dbSNP
Genome
hg19
Position
chr1:11,845,780-11,866,021
Variant Type
snv
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