rs1058932
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1058932(C;C) |
| Make rs1058932(C;T) |
| Make rs1058932(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 95037104 |
| Gene | CYP2C8 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1058932 |
| dbSNP (classic) | rs1058932 |
| ClinGen | rs1058932 |
| ebi | rs1058932 |
| HLI | rs1058932 |
| Exac | rs1058932 |
| Gnomad | rs1058932 |
| Varsome | rs1058932 |
| LitVar | rs1058932 |
| Map | rs1058932 |
| PheGenI | rs1058932 |
| Biobank | rs1058932 |
| 1000 genomes | rs1058932 |
| hgdp | rs1058932 |
| ensembl | rs1058932 |
| geneview | rs1058932 |
| scholar | rs1058932 |
| rs1058932 | |
| pharmgkb | rs1058932 |
| gwascentral | rs1058932 |
| openSNP | rs1058932 |
| 23andMe | rs1058932 |
| SNPshot | rs1058932 |
| SNPdbe | rs1058932 |
| MSV3d | rs1058932 |
| GWAS Ctlg | rs1058932 |
| GMAF | 0.2787 |
| Max Magnitude | 0 |
| ? | (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.
