rs11164838
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | >1.11x risk | |
| (C;T) | 1.11x risk | |
| (T;T) | 0 | common |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 92929821 |
| Gene | FAM69A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11164838 |
| dbSNP (classic) | rs11164838 |
| ClinGen | rs11164838 |
| ebi | rs11164838 |
| HLI | rs11164838 |
| Exac | rs11164838 |
| Gnomad | rs11164838 |
| Varsome | rs11164838 |
| LitVar | rs11164838 |
| Map | rs11164838 |
| PheGenI | rs11164838 |
| Biobank | rs11164838 |
| 1000 genomes | rs11164838 |
| hgdp | rs11164838 |
| ensembl | rs11164838 |
| geneview | rs11164838 |
| scholar | rs11164838 |
| rs11164838 | |
| pharmgkb | rs11164838 |
| gwascentral | rs11164838 |
| openSNP | rs11164838 |
| 23andMe | rs11164838 |
| SNPshot | rs11164838 |
| SNPdbe | rs11164838 |
| MSV3d | rs11164838 |
| GWAS Ctlg | rs11164838 |
| GMAF | 0.4408 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
rs11164838 has been reported in a large study to be associated with multiple sclerosis.
The risk allele (oriented to the dbSNP entry) is (C); the odds ratio associated with this allele is 1.12 (CI 1.05-1.18). [PMID 17660530]
