rs17594362
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs17594362(C;C) |
| Make rs17594362(C;T) |
| Make rs17594362(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 13 |
| Position | 41565109 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17594362 |
| dbSNP (classic) | rs17594362 |
| ClinGen | rs17594362 |
| ebi | rs17594362 |
| HLI | rs17594362 |
| Exac | rs17594362 |
| Gnomad | rs17594362 |
| Varsome | rs17594362 |
| LitVar | rs17594362 |
| Map | rs17594362 |
| PheGenI | rs17594362 |
| Biobank | rs17594362 |
| 1000 genomes | rs17594362 |
| hgdp | rs17594362 |
| ensembl | rs17594362 |
| geneview | rs17594362 |
| scholar | rs17594362 |
| rs17594362 | |
| pharmgkb | rs17594362 |
| gwascentral | rs17594362 |
| openSNP | rs17594362 |
| 23andMe | rs17594362 |
| SNPshot | rs17594362 |
| SNPdbe | rs17594362 |
| MSV3d | rs17594362 |
| GWAS Ctlg | rs17594362 |
| GMAF | 0.1625 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21833088 ]
|
| Trait | Multiple sclerosis |
| Title | Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. |
| Risk Allele | A |
| P-val | 4E-6 |
| Odds Ratio | 1.11 [1.09-1.13] |
