RS41291556 CYP2C19

Drug Response Chr 10:94775415 snv missense variant

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What This Variant Does

"Defines the CYP2C19 variant known as CYP2C19*8. Carriers of the rs41291556(C) allele may have decrea...

Associated Conditions

CYP2C19: no function

Population Frequencies

gnomAD ALL

0.2%

1kG AFR

0.1%

1kG ALL

99.9%

1kG AMR

100%

1kG EAS

100%

1kG EUR

0.3%

1kG SAS

0.1%

Other Variants in CYP2C19