List of variants reported as pathogenic for adrenocortical insufficiency by Institute of Human Genetics, Medical University Innsbruck

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000500.9(CYP21A2):c.1272C>A (p.Cys424Ter)	rs1367112998
NM_000500.9(CYP21A2):c.1291G>A (p.Gly431Ser)	rs1582312633
NM_000500.9(CYP21A2):c.509G>A (p.Cys170Tyr)	rs1582304457
NM_000500.9(CYP21A2):c.525C>A (p.Tyr175Ter)	rs1582304536

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