rs4908760
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;G) | 0 | common in complete genomics |
| Make rs4908760(A;A) |
| Make rs4908760(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 8466082 |
| Gene | RERE |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4908760 |
| dbSNP (classic) | rs4908760 |
| ClinGen | rs4908760 |
| ebi | rs4908760 |
| HLI | rs4908760 |
| Exac | rs4908760 |
| Gnomad | rs4908760 |
| Varsome | rs4908760 |
| LitVar | rs4908760 |
| Map | rs4908760 |
| PheGenI | rs4908760 |
| Biobank | rs4908760 |
| 1000 genomes | rs4908760 |
| hgdp | rs4908760 |
| ensembl | rs4908760 |
| geneview | rs4908760 |
| scholar | rs4908760 |
| rs4908760 | |
| pharmgkb | rs4908760 |
| gwascentral | rs4908760 |
| openSNP | rs4908760 |
| 23andMe | rs4908760 |
| SNPshot | rs4908760 |
| SNPdbe | rs4908760 |
| MSV3d | rs4908760 |
| GWAS Ctlg | rs4908760 |
| GMAF | 0.281 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20410501 ]
|
| Trait | Vitiligo |
| Title | Variant of TYR and Autoimmunity Susceptibility Loci in Generalized Vitiligo |
| Risk Allele | G |
| P-val | 7E-15 |
| Odds Ratio | 1.36 [1.26-1.48] |
