rs5912838
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs5912838(A;A) |
| Make rs5912838(A;C) |
| Make rs5912838(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | X |
| Position | 79241621 |
| Gene | LOC107985690 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs5912838 |
| dbSNP (classic) | rs5912838 |
| ClinGen | rs5912838 |
| ebi | rs5912838 |
| HLI | rs5912838 |
| Exac | rs5912838 |
| Gnomad | rs5912838 |
| Varsome | rs5912838 |
| LitVar | rs5912838 |
| Map | rs5912838 |
| PheGenI | rs5912838 |
| Biobank | rs5912838 |
| 1000 genomes | rs5912838 |
| hgdp | rs5912838 |
| ensembl | rs5912838 |
| geneview | rs5912838 |
| scholar | rs5912838 |
| rs5912838 | |
| pharmgkb | rs5912838 |
| gwascentral | rs5912838 |
| openSNP | rs5912838 |
| 23andMe | rs5912838 |
| SNPshot | rs5912838 |
| SNPdbe | rs5912838 |
| MSV3d | rs5912838 |
| GWAS Ctlg | rs5912838 |
| GMAF | 0.4849 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23612905] |
| Trait | Graves' disease |
| Title | Robust evidence for five new Graves' disease risk loci from a staged genome-wide association analysis. |
| Risk Allele | |
| P-val | 2E-33 |
| Odds Ratio | 1.32 [1.25-1.37] |
[PMID 23667180
] An X chromosome-wide association analysis identifies variants in GPR174 as a risk factor for Graves' disease.
