rs11962089
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11962089(A;A) |
| Make rs11962089(A;G) |
| Make rs11962089(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 105164345 |
| Gene | BVES-AS1, POPDC3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11962089 |
| dbSNP (classic) | rs11962089 |
| ClinGen | rs11962089 |
| ebi | rs11962089 |
| HLI | rs11962089 |
| Exac | rs11962089 |
| Gnomad | rs11962089 |
| Varsome | rs11962089 |
| LitVar | rs11962089 |
| Map | rs11962089 |
| PheGenI | rs11962089 |
| Biobank | rs11962089 |
| 1000 genomes | rs11962089 |
| hgdp | rs11962089 |
| ensembl | rs11962089 |
| geneview | rs11962089 |
| scholar | rs11962089 |
| rs11962089 | |
| pharmgkb | rs11962089 |
| gwascentral | rs11962089 |
| openSNP | rs11962089 |
| 23andMe | rs11962089 |
| SNPshot | rs11962089 |
| SNPdbe | rs11962089 |
| MSV3d | rs11962089 |
| GWAS Ctlg | rs11962089 |
| GMAF | 0.1478 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21654844 ]
|
| Trait | |
| Title | Genome-wide association study of severity in multiple sclerosis. |
| Risk Allele | G |
| P-val | 0.000008 |
| Odds Ratio | 0.6900 [NR] unit decrease |
