RS6471 CYP21A2

Health Risk Chr 6:32040110
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What This Variant Does
"[OMIM:?]
Associated Conditions
ADRENAL HYPERPLASIA
CONGENITAL
DUE TO 21-HYDROXYLASE DEFICIENCY
Carcinoma
adrenocortical
androgen-secreting
Adenoma
cortisol-producing
Inborn genetic diseases
Congenital adrenal hyperplasia
CYP21A2-related disorder
ADRENAL HYPERPLASIA
CONGENITAL
DUE TO 21-HYDROXYLASE DEFICIENCY
Carcinoma
Other Variants in CYP21A2
rs6475 rs9378251 rs6467 rs201552310 rs397509367 rs6445 rs387906510 rs1474566961 rs7755898 rs72552754
Ask Dr. Hemsworth about this variant