RS58973490 CYP2C19

Drug Response Chr 10:94775506 snv missense variant

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What This Variant Does

"The rs58973490(A) SNP defines the CYP2C19 allele known as CYP2C19*11."

Associated Conditions

CYP2C19: normal function

Population Frequencies

gnomAD ALL

99.5%

1kG AFR

0.1%

1kG ALL

0.1%

1kG AMR

100%

1kG EAS

100%

1kG EUR

99.6%

1kG SAS

100%

Other Variants in CYP2C19