RS6467 CYP21A2
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What This Variant Does
"Note that this SNP is unusual in at least two regards. First, it is defined in both dbSNP and here i...
Associated Conditions
ADRENAL HYPERPLASIA
CONGENITAL
DUE TO 21-HYDROXYLASE DEFICIENCY
Inborn genetic diseases
See cases
Congenital adrenal hyperplasia
Ovarian serous cystadenocarcinoma
ADRENAL HYPERPLASIA
CONGENITAL
DUE TO 21-HYDROXYLASE DEFICIENCY
Inborn genetic diseases
See cases
Congenital adrenal hyperplasia
Ovarian serous cystadenocarcinoma
Other Variants in CYP21A2