RS12530380 CYP21A2

Health Risk Chr 6:32039809 snv missense variant
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What This Variant Does
"[OMIM:?]
Associated Conditions
ADRENAL HYPERPLASIA
CONGENITAL
DUE TO 21-HYDROXYLASE DEFICIENCY
Congenital adrenal hyperplasia
ADRENAL HYPERPLASIA
CONGENITAL
DUE TO 21-HYDROXYLASE DEFICIENCY
Congenital adrenal hyperplasia
Population Frequencies
gnomAD ALL
0%
Other Variants in CYP21A2
rs6475 rs6471 rs9378251 rs6467 rs201552310 rs397509367 rs6445 rs387906510 rs1474566961 rs7755898
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