chr3:10285666:> Detail (hg38)

Information

Genome

Assembly Position
hg19 chr3:10,327,350-10,334,631 
hg38 chr3:10,285,666-10,292,947

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
0.002 Cardiovascular Diseases NA GAD Detail
0.003 celiac disease NA LHGDN Detail
0.002 Churg-Strauss syndrome NA GAD Detail
0.120 colitis NA CTD_human Detail
0.120 ulcerative colitis NA CTD_human Detail
0.005 Colonic Neoplasms NA GAD,LHGDN Detail
<0.001 Coronary Arteriosclerosis High plasma ghrelin protects from coronary heart disease and Leu72Leu polymorphi... BeFree 25257375 Detail
0.003 Coronary heart disease High plasma ghrelin protects from coronary heart disease and Leu72Leu polymorphi... BeFree,GAD 25257375 Detail
0.003 Crohn Disease NA LHGDN Detail
0.005 Cushing syndrome NA LHGDN Detail
0.002 Mental Depression NA GAD Detail
0.120 depressive disorder NA CTD_human Detail
0.001 Diabetes NA BeFree Detail
0.004 diabetes mellitus NA BeFree,LHGDN Detail
0.017 Diabetes Mellitus, Non-Insulin-Dependent MTLRP genetic polymorphism (214C>A) was associated with Type 2 diabetes in Cauca... BeFree,GAD,LHGDN 25095788 Detail
0.005 Diabetic Nephropathy NA BeFree,GAD,LHGDN Detail
<0.001 Dwarfism NA BeFree Detail
0.003 Eating Disorders NA BeFree,GAD Detail
0.120 Esophageal Neoplasms NA CTD_human Detail
0.003 Fatty Liver NA LHGDN Detail
0.003 gastritis NA LHGDN Detail
0.003 Gastritis, Atrophic NA LHGDN Detail
0.005 Heart Diseases NA LHGDN Detail
0.121 Heart failure NA BeFree,CTD_human Detail
<0.001 congestive heart failure NA BeFree Detail
0.003 Huntington disease NA LHGDN Detail
0.005 hyperinsulinism NA LHGDN Detail
0.008 Hypertensive disease NA BeFree,GAD,LHGDN Detail
0.003 Hypotension NA LHGDN Detail
<0.001 Infant, Small for Gestational Age Ghrelin and obestatin plasma levels and ghrelin/obestatin prepropeptide gene pol... BeFree 25223427 Detail
0.008 Inflammation NA GAD,LHGDN Detail
0.002 Insulin resistance NA GAD Detail
0.003 Kidney Failure, Chronic NA LHGDN Detail
0.003 liver cirrhosis NA LHGDN Detail
0.003 Biliary cirrhosis NA LHGDN Detail
0.003 Lung Neoplasms NA LHGDN Detail
0.005 Lymphoma, Non-Hodgkin NA GAD Detail
<0.001 Malignant neoplasm of stomach NA BeFree Detail
0.003 myocardial infarction NA BeFree,LHGDN Detail
0.120 Nerve Degeneration NA CTD_human Detail
0.120 Neural Tube Defects NA CTD_human Detail
0.002 Obesity, Morbid NA GAD Detail
<0.001 Ovarian Diseases NA BeFree Detail
<0.001 pancreatitis NA BeFree Detail
0.006 pheochromocytoma NA BeFree,LHGDN Detail
0.001 pituitary adenoma NA BeFree Detail
<0.001 Pituitary Diseases NA BeFree Detail
0.017 polycystic ovary syndrome NA BeFree,LHGDN Detail
0.016 Prader-Willi syndrome NA LHGDN Detail
0.003 Prostatic Neoplasms NA LHGDN Detail
0.002 kidney failure NA GAD Detail
0.120 Reperfusion Injury NA CTD_human Detail
0.003 schizophrenia NA BeFree,GAD Detail
0.120 Seizures NA CTD_human Detail
0.005 Stomach Neoplasms NA LHGDN Detail
0.120 gastric ulcer NA CTD_human Detail
0.002 Tobacco use disorder NA GAD Detail
0.003 uremia NA LHGDN Detail
0.120 Weight Gain NA CTD_human Detail
0.002 gestational diabetes NA GAD Detail
0.005 Malnutrition NA LHGDN Detail
0.003 Neuroendocrine Tumors NA BeFree,LHGDN Detail
0.005 pituitary-dependent Cushing's disease NA LHGDN Detail
0.120 Cocaine-Related Disorders NA CTD_human Detail
0.003 Gastrointestinal Stromal Tumors NA LHGDN Detail
<0.001 Medullary carcinoma of thyroid NA BeFree Detail
<0.001 Chronic heart failure NA BeFree Detail
<0.001 Impaired glucose tolerance NA BeFree Detail
<0.001 Adenocarcinoma Of Esophagus NA BeFree Detail
<0.001 Carcinoid tumor no ICD-O subtype NA BeFree Detail
<0.001 Malignant neoplasm of prostate NA BeFree Detail
<0.001 Overweight NA BeFree Detail
0.005 body mass NA GAD Detail
0.009 Metabolic syndrome X NA BeFree,GAD Detail
0.002 Malignant neoplasm of esophagus NA GAD Detail
<0.001 Thyroid carcinoma NA BeFree Detail
0.003 Eating Disorders No association of the neuropeptide Y (Leu7Pro) and ghrelin gene (Arg51Gln, Leu72... BeFree 21047193 Detail
<0.001 prostate carcinoma NA BeFree Detail
<0.001 heavy drinking NA BeFree Detail
<0.001 stomach carcinoma NA BeFree Detail
0.080 Infarction, Middle Cerebral Artery NA RGD Detail
<0.001 Helicobacter pylori infection NA BeFree Detail
0.002 Microsatellite Instability NA GAD Detail
<0.001 ACTH-secreting pituitary adenoma NA BeFree Detail
0.003 Mammary Neoplasms NA LHGDN Detail
0.002 colorectal cancer NA GAD Detail
0.002 Methamphetamine dependence NA GAD Detail
<0.001 coronary artery disease NA BeFree Detail
0.009 bulimia nervosa NA BeFree,LHGDN Detail
0.002 granulomatosis with polyangiitis NA GAD Detail
0.019 Infection NA LHGDN Detail
0.003 acromegaly NA LHGDN Detail
0.120 adenocarcinoma NA CTD_human Detail
0.003 adenoma NA BeFree,LHGDN Detail
0.005 Alcoholic Intoxication, Chronic NA GAD Detail
0.008 Anorexia NA BeFree,LHGDN Detail
0.017 anorexia nervosa NA BeFree,GAD,LHGDN Detail
0.003 rheumatoid arthritis NA BeFree,LHGDN Detail
0.005 asthma NA BeFree,GAD,LHGDN Detail
0.006 atherosclerosis NA BeFree,LHGDN Detail
0.008 Bulimia NA GAD,LHGDN Detail
0.123 Cachexia NA BeFree,CTD_human,LHGDN Detail
Annotation

Annotations

DescrptionSourceLinks
NA DisGeNET Detail
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High plasma ghrelin protects from coronary heart disease and Leu72Leu polymorphism of ghrelin gene f... DisGeNET Detail
High plasma ghrelin protects from coronary heart disease and Leu72Leu polymorphism of ghrelin gene f... DisGeNET Detail
NA DisGeNET Detail
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MTLRP genetic polymorphism (214C>A) was associated with Type 2 diabetes in Caucasian population: a m... DisGeNET Detail
NA DisGeNET Detail
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Ghrelin and obestatin plasma levels and ghrelin/obestatin prepropeptide gene polymorphisms in small ... DisGeNET Detail
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No association of the neuropeptide Y (Leu7Pro) and ghrelin gene (Arg51Gln, Leu72Met, Gln90Leu) singl... 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
rs386539811 dbSNP
Genome
hg38
Position
chr3:10,285,666-10,292,947
Variant Type
snv
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