RS17879685 CYP2C19

Drug Response Chr 10:94849994 snv missense variant

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What This Variant Does

"The rs17879685(T) SNP defines the CYP2C19 allele known as CYP2C19*13."

Associated Conditions

CYP2C19: normal function

Population Frequencies

gnomAD ALL

100%

1kG AFR

1kG ALL

99.4%

1kG AMR

99.7%

1kG EAS

100%

1kG EUR

100%

1kG SAS

100%

Other Variants in CYP2C19