rs4713693
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4713693(C;C) |
| Make rs4713693(C;T) |
| Make rs4713693(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 33850152 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4713693 |
| dbSNP (classic) | rs4713693 |
| ClinGen | rs4713693 |
| ebi | rs4713693 |
| HLI | rs4713693 |
| Exac | rs4713693 |
| Gnomad | rs4713693 |
| Varsome | rs4713693 |
| LitVar | rs4713693 |
| Map | rs4713693 |
| PheGenI | rs4713693 |
| Biobank | rs4713693 |
| 1000 genomes | rs4713693 |
| hgdp | rs4713693 |
| ensembl | rs4713693 |
| geneview | rs4713693 |
| scholar | rs4713693 |
| rs4713693 | |
| pharmgkb | rs4713693 |
| gwascentral | rs4713693 |
| openSNP | rs4713693 |
| 23andMe | rs4713693 |
| SNPshot | rs4713693 |
| SNPdbe | rs4713693 |
| MSV3d | rs4713693 |
| GWAS Ctlg | rs4713693 |
| GMAF | 0.4151 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21900946] |
| Trait | |
| Title | Identification of independent risk loci for Graves' disease within the MHC in the Japanese population. |
| Risk Allele | T |
| P-val | 7E-13 |
| Odds Ratio | 1.4000 [1.28-1.53] |
