RS1799853 CYP2C9

Drug Response Chr 10:94942289 snv missense variant
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What This Variant Does
"rs1799853 is a SNP in the CYP2C9 gene and is linked to poor warfarin metabolism and risk of GI bleed...
Associated Conditions
Medication Interactions
Warfarin dose_adjustment strong
CYP2C9*2 — reduced metabolism, lower dose needed
Ibuprofen metabolism moderate
CYP2C9*2 — slower NSAID clearance
GWAS Studies (1)
Trait Risk Allele OR / Beta P-value Study
Warfarin maintenance dose OR: 0.54 1E-31 PubMed
Population Frequencies
gnomAD ALL
88.2%
1kG AFR
99.2%
1kG ALL
4.8%
1kG AMR
90.1%
1kG EAS
99.9%
1kG EUR
87.6%
1kG SAS
3.5%
Other Variants in CYP2C9
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