Rs1058932
From SNPedia
| Orientation | minus |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1058932 |
| PheGenI | rs1058932 |
| nextbio | rs1058932 |
| hapmap | rs1058932 |
| 1000 genomes | rs1058932 |
| hgdp | rs1058932 |
| ensembl | rs1058932 |
| gopubmed | rs1058932 |
| geneview | rs1058932 |
| scholar | rs1058932 |
| rs1058932 | |
| pharmgkb | rs1058932 |
| gwascentral | rs1058932 |
| openSNP | rs1058932 |
| 23andMe | rs1058932 |
| 23andMe all | rs1058932 |
| SNP Nexus | |
| SNPshot | rs1058932 |
| SNPdbe | rs1058932 |
| MSV3d | rs1058932 |
| Gene | CYP2C8 |
| Chromosome | 10 |
| Orientation | minus |
| GMAF | 0.2788 |
| Position | 96796861 |
| Reference | GRCh37 37.1/131 |
| Max Magnitude |
| Make rs1058932(C;C) |
| Make rs1058932(C;T) |
| Make rs1058932(T;T) |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
[PMID 20436375] Genetic variance in CYP2C8 and increased risk of myocardial infarction
[PMID 17048007] Association of warfarin dose with genes involved in its action and metabolism.
