rs9332131
From SNPedia
| Warfarin (Coumadin®) |
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (-;-) | 2.5 | CYP2C9*6 homozygote |
| (-;A) | carrier of one CYP2C9*6 allele | |
| (A;A) | 0 | normal |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 94949282 |
| Gene | CYP2C9 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9332131 |
| dbSNP (classic) | rs9332131 |
| ClinGen | rs9332131 |
| ebi | rs9332131 |
| HLI | rs9332131 |
| Exac | rs9332131 |
| Gnomad | rs9332131 |
| Varsome | rs9332131 |
| LitVar | rs9332131 |
| Map | rs9332131 |
| PheGenI | rs9332131 |
| Biobank | rs9332131 |
| 1000 genomes | rs9332131 |
| hgdp | rs9332131 |
| ensembl | rs9332131 |
| geneview | rs9332131 |
| scholar | rs9332131 |
| rs9332131 | |
| pharmgkb | rs9332131 |
| gwascentral | rs9332131 |
| openSNP | rs9332131 |
| 23andMe | rs9332131 |
| SNPshot | rs9332131 |
| SNPdbe | rs9332131 |
| MSV3d | rs9332131 |
| GWAS Ctlg | rs9332131 |
| Max Magnitude | 2.5 |
| This SNP has been recognized by the Coriell Personalized Medicine Collaborative ICOB.
|
rs9332131, also known as 818delA, 10601delA or 273Frame shift, is a SNP in the CYP2C9 gene.
The rs9332131(-) allele defines the CYP2C9*6 variant, which is inactive.
[PMID 20214591] Pharmacogenomics in aspirin intolerance
[PMID 18466099
] Influence of CYP2C9 and VKORC1 on warfarin dose, anticoagulation attainment and maintenance among European-Americans and African-Americans.
[PMID 18752379] Warfarin pharmacogenetics.
[PMID 19955245] Warfarin sensitivity genotyping: a review of the literature and summary of patient experience.
| ClinVar | |
|---|---|
| Risk | Rs9332131(-;-) |
| Alt | Rs9332131(-;-) |
| Reference | Rs9332131(A;A) |
| Significance | Other |
| Disease | not provided |
| Variation | info |
| Gene | CYP2C9 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000010.10:g.96709039delA |
| CLNSRC | |
| CLNACC | RCV000363569.1, |
