rs61839660
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs61839660(C;T) |
| Make rs61839660(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 6052734 |
| Gene | IL2RA |
| is a | snp |
| is | mentioned by |
| dbSNP | rs61839660 |
| dbSNP (classic) | rs61839660 |
| ClinGen | rs61839660 |
| ebi | rs61839660 |
| HLI | rs61839660 |
| Exac | rs61839660 |
| Gnomad | rs61839660 |
| Varsome | rs61839660 |
| LitVar | rs61839660 |
| Map | rs61839660 |
| PheGenI | rs61839660 |
| Biobank | rs61839660 |
| 1000 genomes | rs61839660 |
| hgdp | rs61839660 |
| ensembl | rs61839660 |
| geneview | rs61839660 |
| scholar | rs61839660 |
| rs61839660 | |
| pharmgkb | rs61839660 |
| gwascentral | rs61839660 |
| openSNP | rs61839660 |
| 23andMe | rs61839660 |
| SNPshot | rs61839660 |
| SNPdbe | rs61839660 |
| MSV3d | rs61839660 |
| GWAS Ctlg | rs61839660 |
| GMAF | 0.03398 |
| Max Magnitude | 0 |
| GWAS snp | |
|---|---|
| PMID | [PMID 22293688 ]
|
| Trait | |
| Title | 1000 Genomes-based imputation identifies novel and refined associations for the Wellcome Trust Case Control Consortium phase 1 Data. |
| Risk Allele | |
| P-val | 5E-9 |
| Odds Ratio | 1.6000 None |
