rs7900744
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7900744(A;A) |
| Make rs7900744(A;G) |
| Make rs7900744(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 6023648 |
| Gene | IL2RA |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7900744 |
| dbSNP (classic) | rs7900744 |
| ClinGen | rs7900744 |
| ebi | rs7900744 |
| HLI | rs7900744 |
| Exac | rs7900744 |
| Gnomad | rs7900744 |
| Varsome | rs7900744 |
| LitVar | rs7900744 |
| Map | rs7900744 |
| PheGenI | rs7900744 |
| Biobank | rs7900744 |
| 1000 genomes | rs7900744 |
| hgdp | rs7900744 |
| ensembl | rs7900744 |
| geneview | rs7900744 |
| scholar | rs7900744 |
| rs7900744 | |
| pharmgkb | rs7900744 |
| gwascentral | rs7900744 |
| openSNP | rs7900744 |
| 23andMe | rs7900744 |
| SNPshot | rs7900744 |
| SNPdbe | rs7900744 |
| MSV3d | rs7900744 |
| GWAS Ctlg | rs7900744 |
| GMAF | 0.2332 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| Rs7900744 | |
|---|---|
| PubMed | [PMID 17371467] |
| Affy Probeset | SNP_A-8468428 |
| Affy Orientation | same |
| On GW 5.0 | 0 |
| Alleles A/B | A/G |
| Ancestral | A |
| Population | UK |
| Allele | G |
| Case Freq. | |
| Control Freq. | |
| Odds Ratio Het | |
| Odds Ratio Hom | |
| Odds Ratio All | 1.12 |
| Disease | Graves' Disease (GD) |
[PMID 17371467] a general susceptibility locus for autoimmune disease found via 1896 Graves' disease patients matched to 1822 controls (P = 4.5 x 10(-4)).
rs7900744 is in linkage disequilibrium with a polymorphism that increases susceptibility to Graves' Disease 1.12 times for carriers of the G allele [PMID 17371467]
