rs771767
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs771767(C;C) |
| Make rs771767(C;T) |
| Make rs771767(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 3 |
| Position | 102029794 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs771767 |
| dbSNP (classic) | rs771767 |
| ClinGen | rs771767 |
| ebi | rs771767 |
| HLI | rs771767 |
| Exac | rs771767 |
| Gnomad | rs771767 |
| Varsome | rs771767 |
| LitVar | rs771767 |
| Map | rs771767 |
| PheGenI | rs771767 |
| Biobank | rs771767 |
| 1000 genomes | rs771767 |
| hgdp | rs771767 |
| ensembl | rs771767 |
| geneview | rs771767 |
| scholar | rs771767 |
| rs771767 | |
| pharmgkb | rs771767 |
| gwascentral | rs771767 |
| openSNP | rs771767 |
| 23andMe | rs771767 |
| SNPshot | rs771767 |
| SNPdbe | rs771767 |
| MSV3d | rs771767 |
| GWAS Ctlg | rs771767 |
| GMAF | 0.225 |
| 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 | A |
| P-val | 9E-9 |
| Odds Ratio | 1.1000 [1.09-1.12] |
