RS886038207 CYP21A2;LOC106780800

Health Risk Chr 6:32038580
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What This Variant Does
"CLNSIG=4
Associated Conditions
ADRENAL HYPERPLASIA
CONGENITAL
DUE TO 21-HYDROXYLASE DEFICIENCY
ADRENAL HYPERPLASIA
CONGENITAL
DUE TO 21-HYDROXYLASE DEFICIENCY
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