rs669607
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;T) | 0 | common in complete genomics |
| Make rs669607(G;G) |
| Make rs669607(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 28029953 |
| Gene | LOC107986041 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs669607 |
| dbSNP (classic) | rs669607 |
| ClinGen | rs669607 |
| ebi | rs669607 |
| HLI | rs669607 |
| Exac | rs669607 |
| Gnomad | rs669607 |
| Varsome | rs669607 |
| LitVar | rs669607 |
| Map | rs669607 |
| PheGenI | rs669607 |
| Biobank | rs669607 |
| 1000 genomes | rs669607 |
| hgdp | rs669607 |
| ensembl | rs669607 |
| geneview | rs669607 |
| scholar | rs669607 |
| rs669607 | |
| pharmgkb | rs669607 |
| gwascentral | rs669607 |
| openSNP | rs669607 |
| 23andMe | rs669607 |
| SNPshot | rs669607 |
| SNPdbe | rs669607 |
| MSV3d | rs669607 |
| GWAS Ctlg | rs669607 |
| GMAF | 0.3889 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
23andMe blog multiple sclerosis C 1.15x
| GWAS snp | |
|---|---|
| PMID | [PMID 21833088 ]
|
| Trait | |
| Title | Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. |
| Risk Allele | C |
| P-val | 2E-15 |
| Odds Ratio | 1.1300 [1.12-1.15] |
