rs670659
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs670659(C;C) |
| Make rs670659(C;T) |
| Make rs670659(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 240998475 |
| Gene | RGS7 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs670659 |
| dbSNP (classic) | rs670659 |
| ClinGen | rs670659 |
| ebi | rs670659 |
| HLI | rs670659 |
| Exac | rs670659 |
| Gnomad | rs670659 |
| Varsome | rs670659 |
| LitVar | rs670659 |
| Map | rs670659 |
| PheGenI | rs670659 |
| Biobank | rs670659 |
| 1000 genomes | rs670659 |
| hgdp | rs670659 |
| ensembl | rs670659 |
| geneview | rs670659 |
| scholar | rs670659 |
| rs670659 | |
| pharmgkb | rs670659 |
| gwascentral | rs670659 |
| openSNP | rs670659 |
| 23andMe | rs670659 |
| SNPshot | rs670659 |
| SNPdbe | rs670659 |
| MSV3d | rs670659 |
| GWAS Ctlg | rs670659 |
| GMAF | 0.3365 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
Gene variants associated with deep vein thrombosis.[PMID 18349091]
Updated analysis of gene variants associated with deep vein thrombosis.[PMID 20124536]
[PMID 21232005
] New gene variants associated with venous thrombosis: a replication study in White and Black Americans.
