rs706779
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs706779(A;A) |
| Make rs706779(A;G) |
| Make rs706779(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 6056861 |
| Gene | IL2RA |
| is a | snp |
| is | mentioned by |
| dbSNP | rs706779 |
| dbSNP (classic) | rs706779 |
| ClinGen | rs706779 |
| ebi | rs706779 |
| HLI | rs706779 |
| Exac | rs706779 |
| Gnomad | rs706779 |
| Varsome | rs706779 |
| LitVar | rs706779 |
| Map | rs706779 |
| PheGenI | rs706779 |
| Biobank | rs706779 |
| 1000 genomes | rs706779 |
| hgdp | rs706779 |
| ensembl | rs706779 |
| geneview | rs706779 |
| scholar | rs706779 |
| rs706779 | |
| pharmgkb | rs706779 |
| gwascentral | rs706779 |
| openSNP | rs706779 |
| 23andMe | rs706779 |
| SNPshot | rs706779 |
| SNPdbe | rs706779 |
| MSV3d | rs706779 |
| GWAS Ctlg | rs706779 |
| GMAF | 0.4711 |
| 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 | A |
| P-val | 3E-9 |
| Odds Ratio | 1.27 [1.17-1.37] |
[PMID 18840781] Follow-up analysis of genome-wide association data identifies novel loci for type 1 diabetes.
[PMID 19956101] Overview of the Rapid Response data.
