rs696217
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs696217(G;T) |
| Make rs696217(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 10289773 |
| Gene | GHRL, GHRLOS |
| is a | snp |
| is | mentioned by |
| dbSNP | rs696217 |
| dbSNP (classic) | rs696217 |
| ClinGen | rs696217 |
| ebi | rs696217 |
| HLI | rs696217 |
| Exac | rs696217 |
| Gnomad | rs696217 |
| Varsome | rs696217 |
| LitVar | rs696217 |
| Map | rs696217 |
| PheGenI | rs696217 |
| Biobank | rs696217 |
| 1000 genomes | rs696217 |
| hgdp | rs696217 |
| ensembl | rs696217 |
| geneview | rs696217 |
| scholar | rs696217 |
| rs696217 | |
| pharmgkb | rs696217 |
| gwascentral | rs696217 |
| openSNP | rs696217 |
| 23andMe | rs696217 |
| SNPshot | rs696217 |
| SNPdbe | rs696217 |
| MSV3d | rs696217 |
| GWAS Ctlg | rs696217 |
| Merged from | Rs28939083 |
| GMAF | 0.09045 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 20010782] Influence of ghrelin gene polymorphisms on hypertension and atherosclerotic disease
| ClinVar | |
|---|---|
| Risk | rs696217(T;T) |
| Alt | rs696217(T;T) |
| Reference | Rs696217(G;G) |
| Significance | Other |
| Disease | Obesity Metabolic syndrome |
| Variation | info |
| Gene | GHRLOS GHRL |
| CLNDBN | Obesity, age at onset of Metabolic syndrome, susceptibility to |
| Reversed | 0 |
| HGVS | NC_000003.11:g.10331457G>T |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000005365.2, RCV000005366.2, |
[PMID 16204371] Variants in the ghrelin gene are associated with metabolic syndrome in the Old Order Amish.
[PMID 16921495] Possible role of preproghrelin gene polymorphisms in susceptibility to bulimia nervosa.
[PMID 17357083
] Medical sequencing at the extremes of human body mass.
[PMID 17389697] Examining the candidacy of ghrelin as a gene responsible for variation in adult stature in a United Kingdom population with type 2 diabetes.
[PMID 18249219] Interaction of single nucleotide polymorphisms in ADRB2, ADRB3, TNF, IL6, IGF1R, LIPC, LEPR, and GHRL with physical activity on the risk of type 2 diabetes mellitus and changes in characteristics of the metabolic syndrome: The Finnish Diabetes Prevention Study.
[PMID 18778477] Genomic variation in myeloma: design, content, and initial application of the Bank On A Cure SNP Panel to detect associations with progression-free survival.
[PMID 19041386] Genetic-epidemiological evidence on genes associated with HDL cholesterol levels: a systematic in-depth review.
[PMID 19077438] Analysis of 30 genes (355 SNPS) related to energy homeostasis for association with adiposity in European-American and Yup'ik Eskimo populations.
[PMID 19593725] Association of maternally inherited GNAS alleles with African-American male birth weight.
[PMID 20191112] The Genetics of Anorexia Nervosa: Current Findings and Future Perspectives.
[PMID 20586762] Genetic variation of the ghrelin signaling system in females with severe alcohol dependence.
[PMID 21448464] The ghrelin signalling system is involved in the consumption of sweets.
[PMID 23257630] Preproghrelin gene polymorphisms in obese Japanese women. Minor homozygotes are light eaters, do not prefer protein or fat, and apparently have a poor appetite.
[PMID 25868387] The association between rs4684677 T/A polymorphism in preproghrelin gene and predisposition to autoimmune thyroid diseases in children
[PMID 26059200] Genetic variation of the growth hormone secretagogue receptor gene is associated with alcohol use disorders identification test scores and smoking
[PMID 28481975] The Leu72Met Polymorphism of the Prepro-ghrelin Gene is Associated With Alcohol Consumption and Subjective Responses to Alcohol: Preliminary Findings.
[PMID 33412253] Ghrelin Modulates Dopaminergic Neuron Formation and Attention Deficit Hyperactivity Disorder-like Behaviors: From Animals to Human Models.
