rs11662763
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11662763(C;C) |
| Make rs11662763(C;T) |
| Make rs11662763(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 18 |
| Position | 5857092 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11662763 |
| dbSNP (classic) | rs11662763 |
| ClinGen | rs11662763 |
| ebi | rs11662763 |
| HLI | rs11662763 |
| Exac | rs11662763 |
| Gnomad | rs11662763 |
| Varsome | rs11662763 |
| LitVar | rs11662763 |
| Map | rs11662763 |
| PheGenI | rs11662763 |
| Biobank | rs11662763 |
| 1000 genomes | rs11662763 |
| hgdp | rs11662763 |
| ensembl | rs11662763 |
| geneview | rs11662763 |
| scholar | rs11662763 |
| rs11662763 | |
| pharmgkb | rs11662763 |
| gwascentral | rs11662763 |
| openSNP | rs11662763 |
| 23andMe | rs11662763 |
| SNPshot | rs11662763 |
| SNPdbe | rs11662763 |
| MSV3d | rs11662763 |
| GWAS Ctlg | rs11662763 |
| GMAF | 0.123 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20694011] |
| Trait | |
| Title | Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency |
| Risk Allele | |
| P-val | 0.000005 |
| Odds Ratio | 1.56 [1.30-1.89] |
