rs1058930
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | normal |
| Make rs1058930(C;C) |
| Make rs1058930(C;G) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 10 |
| Position | 95058362 |
| Gene | CYP2C8 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1058930 |
| dbSNP (classic) | rs1058930 |
| ClinGen | rs1058930 |
| ebi | rs1058930 |
| HLI | rs1058930 |
| Exac | rs1058930 |
| Gnomad | rs1058930 |
| Varsome | rs1058930 |
| LitVar | rs1058930 |
| Map | rs1058930 |
| PheGenI | rs1058930 |
| Biobank | rs1058930 |
| 1000 genomes | rs1058930 |
| hgdp | rs1058930 |
| ensembl | rs1058930 |
| geneview | rs1058930 |
| scholar | rs1058930 |
| rs1058930 | |
| pharmgkb | rs1058930 |
| gwascentral | rs1058930 |
| openSNP | rs1058930 |
| 23andMe | rs1058930 |
| SNPshot | rs1058930 |
| SNPdbe | rs1058930 |
| MSV3d | rs1058930 |
| GWAS Ctlg | rs1058930 |
| GMAF | 0.02571 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
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[PMID 19761371
] Cytochrome P450 2C8 pharmacogenetics: a review of clinical studies.
[PMID 20389299
] Pazopanib-induced hyperbilirubinemia is associated with Gilbert's syndrome UGT1A1 polymorphism.
[PMID 23133420
] Pharmacogenomic Diversity among Brazilians: Influence of Ancestry, Self-Reported Color, and Geographical Origin.
