RS7769409 CYP21A2;LOC106780800;TNXB
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What This Variant Does
"[OMIM:?]
Associated Conditions
ADRENAL HYPERPLASIA
CONGENITAL
DUE TO 21-HYDROXYLASE DEFICIENCY
CYP21A2-related disorder
ADRENAL HYPERPLASIA
CONGENITAL
DUE TO 21-HYDROXYLASE DEFICIENCY
CYP21A2-related disorder
Other Variants in CYP21A2;LOC106780800;TNXB