|| CYP2C9*6 homozygote
|| carrier of one CYP2C9*6 allele
, also known as 818delA, 10601delA or 273Frame shift, is a SNP in the CYP2C9
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.