chr7:95297676:> Detail (hg38)

Information

Genome

Assembly Position
hg19 chr7:94,926,988-94,953,844 
hg38 chr7:95,297,676-95,324,532

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
<0.001 squamous cell carcinoma NA BeFree Detail
0.177 Cardiovascular Diseases Paraoxonase 1 (PON1) is a high-density lipoprotein-bound enzyme that hydrolyzes ... BeFree,CTD_human,GAD,LHGDN 24448003 Detail
0.011 Carotid Artery Diseases NA BeFree,GAD Detail
0.003 celiac disease NA BeFree,LHGDN Detail
0.002 intracranial arteriosclerosis NA GAD Detail
0.003 cerebral infarction NA BeFree,GAD Detail
0.014 brain ischemia NA GAD Detail
0.002 Cerebrovascular Disorders NA GAD Detail
0.002 chorioamnionitis NA GAD Detail
0.002 cleft lip NA GAD Detail
0.002 cleft palate NA GAD Detail
<0.001 colitis NA BeFree Detail
0.003 ulcerative colitis NA BeFree,LHGDN Detail
0.002 Connective Tissue Diseases NA GAD Detail
0.120 Constipation NA CTD_human Detail
0.123 coronary artery vasospasm NA BeFree,CTD_human,GAD Detail
0.003 Crohn Disease NA BeFree,LHGDN Detail
<0.001 cystic fibrosis NA BeFree Detail
<0.001 Presenile dementia NA BeFree Detail
0.003 Mental Depression NA BeFree,GAD Detail
0.121 depressive disorder NA BeFree,CTD_human Detail
0.011 Diabetes Mellitus, Insulin-Dependent Can paraoxonase 1 polymorphisms (L55 M and Q192 R) protect children with type 1 ... BeFree,GAD 24793345 Detail
0.071 Diabetes Mellitus, Non-Insulin-Dependent NA BeFree,GAD,LHGDN Detail
0.005 Diabetic Angiopathies NA BeFree,GAD,LHGDN Detail
0.004 Diabetic Nephropathy NA BeFree,LHGDN Detail
0.130 diabetic retinopathy NA BeFree,CTD_human,GAD Detail
0.009 DNA Damage NA GAD Detail
0.003 endometriosis NA LHGDN Detail
0.002 Fetal Diseases NA GAD Detail
0.002 Fetal Growth Retardation NA GAD Detail
0.002 Fetal Membranes, Premature Rupture NA GAD Detail
0.003 Fibrosis NA LHGDN Detail
<0.001 Gastrointestinal Diseases NA BeFree Detail
0.005 generalized atherosclerosis NA GAD Detail
0.003 Glaucoma, Open-Angle NA BeFree,LHGDN Detail
0.003 glomerulonephritis NA BeFree,GAD Detail
0.003 IgA glomerulonephritis NA BeFree,GAD Detail
0.123 Glomerulonephritis, Membranoproliferative NA BeFree,CTD_human,LHGDN Detail
0.005 Focal glomerulosclerosis NA BeFree,GAD Detail
0.001 Chronic Kidney Diseases The Chi-square test, multivariable logistic regression analysis with adjustment ... BeFree 19578796 Detail
0.002 Head and Neck Neoplasms NA GAD Detail
<0.001 Hemoglobinopathies NA BeFree Detail
0.120 Hemorrhoids NA BeFree,CTD_human Detail
<0.001 Hepatitis, Chronic NA BeFree Detail
0.003 hepatitis C NA LHGDN Detail
<0.001 HIV Infections NA BeFree Detail
<0.001 Hodgkin Disease NA BeFree Detail
<0.001 Huntington disease NA BeFree Detail
0.130 Hypercholesterolemia NA BeFree,CTD_human,GAD Detail
0.125 Hypercholesterolemia, Familial NA BeFree,CTD_human,LHGDN Detail
0.003 Hyperemesis Gravidarum NA LHGDN Detail
0.003 hyperglycemia NA LHGDN Detail
0.009 Hyperlipidemia NA BeFree,GAD,LHGDN Detail
0.003 Hyperlipidemia, Familial Combined NA BeFree,LHGDN Detail
0.200 Hyperlipoproteinemias NA CTD_human,RGD Detail
0.022 Hypertensive disease NA BeFree,GAD,LHGDN Detail
0.120 hyperthyroidism NA CTD_human Detail
0.121 male infertility We speculate that the low activity of PON1 can be a risk factor for male inferti... BeFree,CTD_human 25264968 Detail
0.017 Inflammation NA GAD,LHGDN Detail
0.003 Inflammatory Bowel Diseases NA BeFree,LHGDN Detail
0.007 Insulin resistance NA GAD Detail
0.003 ischemia NA BeFree,LHGDN Detail
0.006 Kidney Diseases NA BeFree,GAD Detail
0.008 Kidney Failure, Chronic NA BeFree,GAD,LHGDN Detail
0.002 Premature Obstetric Labor NA GAD Detail
<0.001 leukemia NA BeFree Detail
<0.001 Leukemia, Myelocytic, Acute NA BeFree Detail
<0.001 liver cirrhosis NA BeFree Detail
0.006 Liver diseases NA BeFree,GAD,LHGDN Detail
<0.001 Liver neoplasms NA BeFree Detail
<0.001 Chronic Obstructive Airway Disease NA BeFree Detail
0.120 Lung Neoplasms NA CTD_human Detail
0.006 Lupus Erythematosus, Systemic NA BeFree,GAD Detail
0.003 lupus nephritis NA BeFree,GAD Detail
0.121 lymphoma NA BeFree,CTD_human Detail
0.005 Lymphoma, Non-Hodgkin NA GAD Detail
<0.001 macular degeneration NA BeFree Detail
0.002 Meningeal Neoplasms NA GAD Detail
0.003 meningioma NA BeFree,GAD Detail
<0.001 Microangiopathy, Diabetic NA BeFree Detail
0.002 Mouth Diseases NA GAD Detail
0.003 multiple myeloma NA BeFree,GAD Detail
0.009 multiple sclerosis NA BeFree,GAD,LHGDN Detail
0.002 Musculoskeletal Diseases NA GAD Detail
0.049 myocardial infarction NA BeFree,GAD,LHGDN Detail
0.002 Neoplasm Recurrence, Local NA GAD Detail
<0.001 Embryonal Neoplasm PON1 rs662>Q192R polymorphism (rs662) is associated with childhood embryonal tum... BeFree 24972570 Detail
0.002 Neoplasms, Glandular and Epithelial NA GAD Detail
0.120 Occupational Diseases NA CTD_human Detail
0.005 Bone necrosis NA GAD,LHGDN Detail
<0.001 ovarian carcinoma NA BeFree Detail
<0.001 Ovarian Diseases NA BeFree Detail
0.002 pancreatitis NA GAD Detail
<0.001 panic disorder Paraoxonase1 192 (PON1 192) gene polymorphism and serum paraoxonase activity in ... BeFree 25600530 Detail
0.020 Parkinson disease NA BeFree,GAD,LHGDN Detail
<0.001 periodontitis NA BeFree Detail
<0.001 placental insufficiency NA BeFree Detail
0.009 polycystic ovary syndrome Lactonase activity and status of paraoxonase 1 in Chinese women with polycystic ... BeFree,GAD,LHGDN 25575948 Detail
0.009 polycystic ovary syndrome PON1 polymorphisms are associated with polycystic ovary syndrome susceptibility,... BeFree,GAD,LHGDN 25956367 Detail
0.010 pre-eclampsia NA GAD,LHGDN Detail
0.002 Pregnancy Complications, Hematologic NA GAD Detail
0.125 Prostatic Neoplasms NA CTD_human,LHGDN Detail
<0.001 psoriasis NA BeFree Detail
0.001 Retinal Diseases NA BeFree Detail
0.003 sarcoidosis NA LHGDN Detail
0.005 schizophrenia NA BeFree,GAD Detail
0.002 Dermatologic disorders NA GAD Detail
0.003 Spasm NA LHGDN Detail
<0.001 ankylosing spondylitis Functional and bioinformatic analyses of single nucleotide polymorphism (SNP) id... BeFree 25989359 Detail
0.048 Cerebrovascular accident NA BeFree,GAD,LHGDN Detail
<0.001 thromboangiitis obliterans NA BeFree Detail
0.002 thrombosis NA GAD Detail
0.002 Tobacco use disorder NA GAD Detail
<0.001 Attention Deficit Disorder NA BeFree Detail
<0.001 Unipolar Depression NA BeFree Detail
0.003 uremia NA BeFree,GAD Detail
0.012 Vascular Diseases NA BeFree,GAD Detail
0.002 Virilism NA GAD Detail
<0.001 Virus Diseases NA BeFree Detail
<0.001 B-Cell Lymphomas NA BeFree Detail
<0.001 T-Cell Lymphoma NA BeFree Detail
0.123 spina bifida NA BeFree,CTD_human,GAD Detail
<0.001 motor neuron disease NA BeFree Detail
<0.001 Peripheral Vascular Diseases NA BeFree Detail
<0.001 severe combined immunodeficiency NA BeFree Detail
0.002 Neoplasms, Second Primary NA GAD Detail
<0.001 acute leukemia NA BeFree Detail
<0.001 Depressive Symptoms NA BeFree Detail
0.005 Pancreatitis, Chronic NA BeFree,GAD,LHGDN Detail
0.003 Left Ventricular Hypertrophy NA LHGDN Detail
<0.001 Small cell carcinoma of lung NA BeFree Detail
<0.001 Migraine Disorders NA BeFree Detail
0.012 Premature Birth NA GAD Detail
0.010 Myocardial Ischemia NA BeFree,GAD Detail
0.002 Malignant neoplasm of brain NA GAD Detail
0.003 Lipid Metabolism Disorders NA BeFree,GAD Detail
<0.001 acute myocardial infarction NA BeFree Detail
<0.001 Disease of capillaries NA BeFree Detail
<0.001 Vascular anomaly Polymorphisms in the genes encoding for enzymes involved in the antioxidant syst... BeFree 26122242 Detail
<0.001 Malnutrition NA BeFree Detail
0.002 Aortic Aneurysm, Abdominal NA GAD Detail
<0.001 Microvascular Angina NA BeFree Detail
0.002 hyperandrogenism NA GAD Detail
<0.001 Diabetic Foot NA BeFree Detail
0.120 Neuroectodermal Tumor, Primitive NA CTD_human Detail
0.005 childhood brain tumor NA GAD Detail
<0.001 Congenital defects NA BeFree Detail
<0.001 Fibrillation NA BeFree Detail
<0.001 Neurologic Symptoms NA BeFree Detail
0.120 Neurotoxicity Syndromes NA CTD_human Detail
0.002 Substance-Related Disorders NA GAD Detail
0.003 coronary stenosis NA BeFree,GAD Detail
<0.001 Dyslipidemias NA BeFree Detail
0.003 Erectile dysfunction NA LHGDN Detail
0.003 Malignant neoplasm of lung Interactions between paraoxonase 1 genetic polymorphisms and smoking and their e... BeFree,GAD 25741997 Detail
0.013 age related macular degeneration NA BeFree,GAD Detail
<0.001 Drug usage NA BeFree Detail
0.007 Oxidative Stress NA GAD Detail
0.007 multiple chemical sensitivity NA GAD Detail
<0.001 Carcinoma, Lewis Lung NA BeFree Detail
<0.001 Chronic colitis NA BeFree Detail
<0.001 essential tremor NA BeFree Detail
<0.001 Impaired glucose tolerance NA BeFree Detail
<0.001 Hemoglobin C trait NA BeFree Detail
0.002 Pesticide poisoning NA GAD Detail
0.121 persian gulf syndrome NA BeFree,CTD_human Detail
0.002 Arsenic Poisoning NA GAD Detail
0.005 Restenosis NA BeFree,GAD Detail
<0.001 Segmental glomerulosclerosis NA BeFree Detail
<0.001 Chronic liver disease NA BeFree Detail
0.003 Complications of Diabetes Mellitus NA LHGDN Detail
<0.001 Primary hypercholesterolemia NA BeFree Detail
0.002 Cardiac Death NA GAD Detail
0.008 Malignant neoplasm of prostate We illustrate the proposed method through three meta-analyses for comparison of ... BeFree,GAD 25363629 Detail
0.120 Hematologic Neoplasms NA CTD_human Detail
0.002 Pancreatitis, Alcoholic NA GAD Detail
<0.001 Hereditary hemochromatosis NA BeFree Detail
<0.001 Chronic constipation NA BeFree Detail
0.001 Chronic Kidney Insufficiency NA BeFree Detail
0.003 Osteoarthritis, Knee NA LHGDN Detail
<0.001 neuropathy NA BeFree Detail
0.006 dementia NA BeFree,GAD,LHGDN Detail
<0.001 Neurodegenerative Disorders NA BeFree Detail
0.003 Hepatitis C, Chronic NA BeFree,GAD Detail
0.009 multiple sclerosis Glyoxalase I A111E, paraoxonase 1 Q192R and L55M polymorphisms: susceptibility f... BeFree 17463067 Detail
<0.001 Cavernous Hemangioma of Brain The present study aimed to investigate the possible association of GLO1 A111E, P... BeFree 26122242 Detail
0.005 Carotid Atherosclerosis NA BeFree,GAD Detail
<0.001 Double coronary vessel disease NA BeFree Detail
0.121 male infertility The results indicated that the PON1 Arg192Glu (rs662) and SOD2 Val16Ala (rs4880)... BeFree 22206979 Detail
0.123 hyperhomocysteinemia NA BeFree,CTD_human,GAD Detail
0.001 prostate carcinoma We illustrate the proposed method through three meta-analyses for comparison of ... BeFree 25363629 Detail
<0.001 Epithelial ovarian cancer NA BeFree Detail
0.003 breast carcinoma NA BeFree Detail
<0.001 Carcinoma of lung Interactions between paraoxonase 1 genetic polymorphisms and smoking and their e... BeFree 25741997 Detail
<0.001 heavy drinking NA BeFree Detail
0.132 Organophosphate poisoning NA CTD_human,GAD Detail
<0.001 Anxiety state NA BeFree Detail
<0.001 Microalbuminuria NA BeFree Detail
<0.001 hyperuricemia NA BeFree Detail
<0.001 cardiac event NA BeFree Detail
0.002 Hypoxia-Ischemia, Brain NA GAD Detail
<0.001 bipolar I disorder NA BeFree Detail
<0.001 Endothelial dysfunction NA BeFree Detail
0.120 Drug-Induced Liver Injury NA CTD_human Detail
<0.001 Cerebral Arteriosclerosis NA BeFree Detail
<0.001 Beta thalassemia trait NA BeFree Detail
0.005 ovarian neoplasm NA GAD,LHGDN Detail
0.011 Ischemic stroke NA BeFree,GAD Detail
0.128 Acute coronary syndrome Alteration of HDL functionality and PON1 activities in acute coronary syndrome p... BeFree,CTD_human,GAD 25218815 Detail
0.003 Malignant neoplasm of ovary NA BeFree,GAD Detail
0.002 Stenosis NA GAD Detail
<0.001 attention deficit hyperactivity disorder NA BeFree Detail
<0.001 major depressive disorder NA BeFree Detail
0.002 Systemic arterial pressure NA GAD Detail
<0.001 Anxiety neurosis (finding) NA BeFree Detail
<0.001 childhood leukemia NA BeFree Detail
0.003 Mammary Neoplasms NA LHGDN Detail
<0.001 Autism Spectrum Disorders NA BeFree Detail
0.001 Chronic Kidney Diseases NA BeFree Detail
0.002 Renal Insufficiency NA GAD Detail
<0.001 Cirrhosis NA BeFree Detail
<0.001 Benign Prostatic Hyperplasia NA BeFree Detail
<0.001 Peripheral Arterial Diseases NA BeFree Detail
0.002 Venous thromboembolism NA GAD Detail
0.120 AMYOTROPHIC LATERAL SCLEROSIS 1 NA CTD_human Detail
0.001 Amyotrophic Lateral Sclerosis, Sporadic NA BeFree Detail
<0.001 PANIC DISORDER 1 Paraoxonase1 192 (PON1 192) gene polymorphism and serum paraoxonase activity in ... BeFree 25600530 Detail
<0.001 Congenital vascular anomaly Polymorphisms in the genes encoding for enzymes involved in the antioxidant syst... BeFree 26122242 Detail
<0.001 liver carcinoma NA BeFree Detail
<0.001 Pediatric Obesity NA BeFree Detail
0.041 Alzheimer's disease Synergistic epistasis of paraoxonase 1 (rs662 and rs85460) and apolipoprotein E4... BeFree 24965284 Detail
<0.001 Alcoholic Steatohepatitis NA BeFree Detail
0.006 Dementia, Vascular Synergistic epistasis of paraoxonase 1 (rs662 and rs85460) and apolipoprotein E4... BeFree 24965284 Detail
0.002 Infection of amniotic sac and membranes, unspecified, unspecified trimester, not applicable or unspecified NA GAD Detail
<0.001 Prostate cancer, familial NA BeFree Detail
<0.001 Three Vessel Coronary Disease NA BeFree Detail
0.003 Ischemic Cerebrovascular Accident NA BeFree Detail
<0.001 Homocysteinemia NA BeFree Detail
0.008 Infection NA GAD,LHGDN Detail
<0.001 Congenital Abnormality NA BeFree Detail
0.002 Spontaneous abortion NA GAD Detail
0.002 congenital adrenal hyperplasia NA GAD Detail
0.125 Agricultural Workers' Diseases NA CTD_human,GAD Detail
0.002 Albuminuria NA GAD Detail
0.003 anemia NA BeFree,LHGDN Detail
0.002 Angina Pectoris NA GAD Detail
<0.001 Angina, Unstable NA BeFree Detail
<0.001 Fabry disease NA BeFree Detail
0.003 Anxiety Disorders NA BeFree,GAD Detail
0.027 arteriosclerosis PON protein expression is present in human aortic tissue and it plays an importa... BeFree 24918121 Detail
0.120 Arteritis NA CTD_human Detail
0.131 rheumatoid arthritis We found that PON-1-Q192R was associated with severity of RA [remission-to-low a... BeFree,CTD_human,GAD,LHGDN 25179377 Detail
0.131 rheumatoid arthritis Anti-cyclic citrullinated peptide antibodies and paraoxonase-1 polymorphism in r... BeFree,CTD_human,GAD,LHGDN 25406539 Detail
0.003 asthma NA BeFree,GAD Detail
0.003 Astrocytoma NA BeFree,GAD Detail
0.203 atherosclerosis PON protein expression is present in human aortic tissue and it plays an importa... BeFree,CTD_human,GAD,LHGDN 24918121 Detail
0.120 autistic disorder NA BeFree,CTD_human Detail
0.006 beta thalassemia NA BeFree,LHGDN Detail
0.120 Birth Weight NA CTD_human Detail
0.003 Malignant neoplasm of urinary bladder NA BeFree,GAD Detail
0.123 Brain Neoplasms NA BeFree,CTD_human,GAD Detail
0.010 Malignant neoplasm of breast NA BeFree,GAD Detail
<0.001 Noninfiltrating Intraductal Carcinoma NA BeFree Detail
Annotation

Annotations

DescrptionSourceLinks
NA DisGeNET Detail
Paraoxonase 1 (PON1) is a high-density lipoprotein-bound enzyme that hydrolyzes toxic oxidized lipid... DisGeNET Detail
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Can paraoxonase 1 polymorphisms (L55 M and Q192 R) protect children with type 1 diabetes against lip... DisGeNET Detail
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The Chi-square test, multivariable logistic regression analysis with adjustment for covariates, and ... DisGeNET Detail
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We speculate that the low activity of PON1 can be a risk factor for male infertility probably due to... DisGeNET Detail
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PON1 rs662>Q192R polymorphism (rs662) is associated with childhood embryonal tumors. DisGeNET Detail
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Paraoxonase1 192 (PON1 192) gene polymorphism and serum paraoxonase activity in panic disorder patie... DisGeNET Detail
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Lactonase activity and status of paraoxonase 1 in Chinese women with polycystic ovarian syndrome. DisGeNET Detail
PON1 polymorphisms are associated with polycystic ovary syndrome susceptibility, related traits, and... DisGeNET Detail
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Functional and bioinformatic analyses of single nucleotide polymorphism (SNP) identified functional ... DisGeNET Detail
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Polymorphisms in the genes encoding for enzymes involved in the antioxidant systems such as glyoxala... DisGeNET Detail
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Interactions between paraoxonase 1 genetic polymorphisms and smoking and their effects on oxidative ... DisGeNET Detail
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We illustrate the proposed method through three meta-analyses for comparison of prostate cancer trea... DisGeNET Detail
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Glyoxalase I A111E, paraoxonase 1 Q192R and L55M polymorphisms: susceptibility factors of multiple s... DisGeNET Detail
The present study aimed to investigate the possible association of GLO1 A111E, PON1 Q192R and L55M p... DisGeNET Detail
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The results indicated that the PON1 Arg192Glu (rs662) and SOD2 Val16Ala (rs4880) variant genotypes w... DisGeNET Detail
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We illustrate the proposed method through three meta-analyses for comparison of prostate cancer trea... DisGeNET Detail
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Interactions between paraoxonase 1 genetic polymorphisms and smoking and their effects on oxidative ... DisGeNET Detail
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Alteration of HDL functionality and PON1 activities in acute coronary syndrome patients. DisGeNET Detail
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Paraoxonase1 192 (PON1 192) gene polymorphism and serum paraoxonase activity in panic disorder patie... DisGeNET Detail
Polymorphisms in the genes encoding for enzymes involved in the antioxidant systems such as glyoxala... DisGeNET Detail
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Synergistic epistasis of paraoxonase 1 (rs662 and rs85460) and apolipoprotein E4 genes in pathogenes... DisGeNET Detail
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Synergistic epistasis of paraoxonase 1 (rs662 and rs85460) and apolipoprotein E4 genes in pathogenes... DisGeNET Detail
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PON protein expression is present in human aortic tissue and it plays an important role in the progr... DisGeNET Detail
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We found that PON-1-Q192R was associated with severity of RA [remission-to-low and moderate-to-high ... DisGeNET Detail
Anti-cyclic citrullinated peptide antibodies and paraoxonase-1 polymorphism in rheumatoid arthritis. DisGeNET Detail
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PON protein expression is present in human aortic tissue and it plays an important role in the progr... DisGeNET Detail
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Overlapped Transcript Coordinates

Gene Transcript ID Exon Number Chromosome Start Stop Type Amino Mutation Transcript Position Links

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs386572987 dbSNP
Genome
hg38
Position
chr7:95,297,676-95,324,532
Variant Type
snv
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