List of variants reported as likely pathogenic for primary adrenal insufficiency by Neuberg Centre For Genomic Medicine, NCGM

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_000102.4(CYP17A1):c.157TTC[1] (p.Phe54del)	rs121434319
NM_000349.3(STAR):c.135del (p.Ser46fs)	rs193922393
NM_000475.5(NR0B1):c.617del (p.His206fs)
NM_000497.4(CYP11B1):c.798C>G (p.Tyr266Ter)
NM_000500.9(CYP21A2):c.1174G>A (p.Ala392Thr)	rs202242769
NM_000529.2(MC2R):c.548dup (p.Leu184fs)
NM_000529.2(MC2R):c.681_688dup (p.Phe230fs)	rs1567895448

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