List of variants reported as pathogenic for adrenocortical insufficiency by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000500.9(CYP21A2):c.1447C>T (p.Pro483Ser)	rs776989258	0.00047
NM_001379228.1(MRAP):c.3G>A (p.Met1Ile)	rs80358231	0.00009
NM_000497.4(CYP11B1):c.1269T>G (p.Tyr423Ter)	rs267606755	0.00001
NM_000500.9(CYP21A2):c.844G>T (p.Val282Leu)	rs6471
NM_015665.6(AAAS):c.1144_1147del (p.Ser382fs)	rs770214071

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