RS12769205 CYP2C19

Drug Response Chr 10:94775366 snv splice acceptor variant
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What This Variant Does
"The CYP2C19 Intron 2 Branch Point SNP is the Ancestral Polymorphism Contributing to the Poor Metabolizer Phenotype in Livers with CYP2C19*35 and CYP2C19*2 Alleles"
Associated Conditions
CYP2C19: no function
CYP2C19: no function
Population Frequencies
gnomAD ALL
83.6%
1kG AFR
80.3%
1kG ALL
22.8%
1kG AMR
10.5%
1kG EAS
68.8%
1kG EUR
85.5%
1kG SAS
64.2%
Other Variants in CYP2C19
rs370803989 rs1564656981 rs145328984 rs1564660997 rs118203756 rs1288601658 rs58973490 rs140278421 rs55640102 rs118203759
Ask Dr. Hemsworth about this variant