rs509035
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs509035(A;A) |
| Make rs509035(A;G) |
| Make rs509035(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 172445659 |
| Gene | GHSR |
| is a | snp |
| is | mentioned by |
| dbSNP | rs509035 |
| dbSNP (classic) | rs509035 |
| ClinGen | rs509035 |
| ebi | rs509035 |
| HLI | rs509035 |
| Exac | rs509035 |
| Gnomad | rs509035 |
| Varsome | rs509035 |
| LitVar | rs509035 |
| Map | rs509035 |
| PheGenI | rs509035 |
| Biobank | rs509035 |
| 1000 genomes | rs509035 |
| hgdp | rs509035 |
| ensembl | rs509035 |
| geneview | rs509035 |
| scholar | rs509035 |
| rs509035 | |
| pharmgkb | rs509035 |
| gwascentral | rs509035 |
| openSNP | rs509035 |
| 23andMe | rs509035 |
| SNPshot | rs509035 |
| SNPdbe | rs509035 |
| MSV3d | rs509035 |
| GWAS Ctlg | rs509035 |
| GMAF | 0.2727 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 19593725
] Association of maternally inherited GNAS alleles with African-American male birth weight.
[PMID 20404923] Family and population-based studies of variation within the ghrelin receptor locus in relation to measures of obesity.
[PMID 21269581] Analysis of the influence of the ghrelin receptor rs509035, rs512692 and rs2922126 polymorphisms in the risk of cardiovascular disease in patients with rheumatoid arthritis.
