RS7755898 CYP21A2

Health Risk Chr 6:32040421
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What This Variant Does
"This SNP is supposed to serve as a marker for the Q318X null allele of the 21-hydroxylase gene. This...
Associated Conditions
ADRENAL HYPERPLASIA
CONGENITAL
DUE TO 21-HYDROXYLASE DEFICIENCY
Congenital adrenal hyperplasia
CYP21A2-related disorder
ADRENAL HYPERPLASIA
CONGENITAL
DUE TO 21-HYDROXYLASE DEFICIENCY
Congenital adrenal hyperplasia
CYP21A2-related disorder
Other Variants in CYP21A2
rs6475 rs6471 rs9378251 rs6467 rs201552310 rs397509367 rs6445 rs387906510 rs1474566961 rs72552754
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