rs7255066
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7255066(C;C) |
| Make rs7255066(C;T) |
| Make rs7255066(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 19 |
| Position | 44642803 |
| Gene | LOC107985305, PVR |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7255066 |
| dbSNP (classic) | rs7255066 |
| ClinGen | rs7255066 |
| ebi | rs7255066 |
| HLI | rs7255066 |
| Exac | rs7255066 |
| Gnomad | rs7255066 |
| Varsome | rs7255066 |
| LitVar | rs7255066 |
| Map | rs7255066 |
| PheGenI | rs7255066 |
| Biobank | rs7255066 |
| 1000 genomes | rs7255066 |
| hgdp | rs7255066 |
| ensembl | rs7255066 |
| geneview | rs7255066 |
| scholar | rs7255066 |
| rs7255066 | |
| pharmgkb | rs7255066 |
| gwascentral | rs7255066 |
| openSNP | rs7255066 |
| 23andMe | rs7255066 |
| SNPshot | rs7255066 |
| SNPdbe | rs7255066 |
| MSV3d | rs7255066 |
| GWAS Ctlg | rs7255066 |
| GMAF | 0.4614 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21833088 ]
|
| Trait | |
| Title | Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. |
| Risk Allele | G |
| P-val | 0.000001 |
| Odds Ratio | 1.0900 [1.07-1.11] |
