rs9332239
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | normal |
| (C;T) | carrier of one CYP2C9*12 allele | |
| (T;T) | CYP2C9*12 homozygote |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 94989020 |
| Gene | CYP2C9 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9332239 |
| dbSNP (classic) | rs9332239 |
| ClinGen | rs9332239 |
| ebi | rs9332239 |
| HLI | rs9332239 |
| Exac | rs9332239 |
| Gnomad | rs9332239 |
| Varsome | rs9332239 |
| LitVar | rs9332239 |
| Map | rs9332239 |
| PheGenI | rs9332239 |
| Biobank | rs9332239 |
| 1000 genomes | rs9332239 |
| hgdp | rs9332239 |
| ensembl | rs9332239 |
| geneview | rs9332239 |
| scholar | rs9332239 |
| rs9332239 | |
| pharmgkb | rs9332239 |
| gwascentral | rs9332239 |
| openSNP | rs9332239 |
| 23andMe | rs9332239 |
| SNPshot | rs9332239 |
| SNPdbe | rs9332239 |
| MSV3d | rs9332239 |
| GWAS Ctlg | rs9332239 |
| GMAF | 0.001837 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
rs9332239, also known as 1465C>T, 50338C>T or P489S, is a SNP in the CYP2C9 gene.
The rs9332239(T) allele defines the CYP2C9*12 variant.
According to a 23andMe discussion This is one of the SNPs which were re-analyzed April 2009. Customers with older data may wish to redownload. SNPs effected rs4420638, rs34276300, rs3091244, rs34601266, rs2033003, rs7900194, rs9332239, rs28371685, rs1229984, and rs28399504.
[PMID 23688605] First report of warfarin dose requirements in patients possessing the CYP2C9*12 allele.
