RS17884712 CYP2C19

Drug Response Chr 10:94775488 snv missense variant
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What This Variant Does
"The rs17884712(A) allele defines the CYP2C19 variant known as CYP2C19*9, which is associated with a ..."
Associated Conditions
CYP2C19: decreased function
CYP2C19: decreased function
Population Frequencies
gnomAD ALL
100%
1kG AFR
1%
1kG ALL
0.3%
1kG AMR
0.1%
1kG EAS
100%
1kG EUR
100%
1kG SAS
100%
Other Variants in CYP2C19
rs370803989 rs145328984 rs1564660997 rs118203756 rs1288601658 rs12769205 rs58973490 rs140278421 rs55640102 rs118203759
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