RS1057910 CYP2C9

Drug Response Chr 10:94981295 snv missense variant
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What This Variant Does
"SNP rs1057910(A), located in the cytochrome p450 CYP2C9 gene, most commonly encodes the amino acid i...
Associated Conditions
Medication Interactions
Warfarin dose_adjustment strong
CYP2C9*3 — significantly reduced metabolism
GWAS Studies (1)
Trait Risk Allele OR / Beta P-value Study
Warfarin maintenance dose OR: 1.11 3E-79 PubMed
ClinVar Assertions (2)
NM_000771.3(CYP2C9):c.[430C=;1075A>C]
· 1 submitter
CYP2C9*3
· 11 submitters
Population Frequencies
gnomAD ALL
6.5%
1kG AFR
99.8%
1kG ALL
95.1%
1kG AMR
3.7%
1kG EAS
3.4%
1kG EUR
7.3%
1kG SAS
10.9%
Other Variants in CYP2C9
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