rs12101261
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs12101261(C;C) |
| Make rs12101261(C;T) |
| Make rs12101261(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 14 |
| Position | 80984885 |
| Gene | TSHR |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12101261 |
| dbSNP (classic) | rs12101261 |
| ClinGen | rs12101261 |
| ebi | rs12101261 |
| HLI | rs12101261 |
| Exac | rs12101261 |
| Gnomad | rs12101261 |
| Varsome | rs12101261 |
| LitVar | rs12101261 |
| Map | rs12101261 |
| PheGenI | rs12101261 |
| Biobank | rs12101261 |
| 1000 genomes | rs12101261 |
| hgdp | rs12101261 |
| ensembl | rs12101261 |
| geneview | rs12101261 |
| scholar | rs12101261 |
| rs12101261 | |
| pharmgkb | rs12101261 |
| gwascentral | rs12101261 |
| openSNP | rs12101261 |
| 23andMe | rs12101261 |
| SNPshot | rs12101261 |
| SNPdbe | rs12101261 |
| MSV3d | rs12101261 |
| GWAS Ctlg | rs12101261 |
| GMAF | 0.4449 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21841780] |
| Trait | |
| Title | A genome-wide association study identifies two new risk loci for Graves' disease. |
| Risk Allele | T |
| P-val | 7E-24 |
| Odds Ratio | 1.3500 [1.28-1.43] |
