List of variants reported as likely benign for primary adrenal insufficiency by Institute of Human Genetics, Medical University Innsbruck

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000500.9(CYP21A2):c.203-46C>T	rs6452	0.01305
NM_000500.9(CYP21A2):c.292+56T>G	rs543633765	0.00139
NM_000500.9(CYP21A2):c.292+37T>A	rs184177366	0.00058
NM_000500.9(CYP21A2):c.292+45_292+46insTGT	rs1422458709
NM_000500.9(CYP21A2):c.293-136C>T	rs1582301685

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