List of variants reported as not provided for primary adrenal insufficiency by GeneReviews

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		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_000500.9(CYP21A2):c.308G>A (p.Arg103Lys)	rs6474	0.25928
NM_000500.9(CYP21A2):c.806G>C (p.Ser269Thr)	rs6472	0.13352
NM_000500.9(CYP21A2):c.1360C>T (p.Pro454Ser)	rs6445	0.00530
NM_000500.7(CYP21A2):c.955C>T (p.Gln319Ter)	rs7755898	0.00339
NM_000500.9(CYP21A2):c.518T>A (p.Ile173Asn)	rs6475	0.00117
NM_000500.9(CYP21A2):c.92C>T (p.Pro31Leu)	rs9378251	0.00055
NM_001395413.1(POR):c.850G>C (p.Ala284Pro)	rs121912974	0.00023
NM_000500.9(CYP21A2):c.1069C>T (p.Arg357Trp)	rs7769409	0.00007
NM_001395413.1(POR):c.1361G>A (p.Arg454His)	rs28931608	0.00005
NM_000500.9(CYP21A2):c.1482C>T (p.Ser494=)	rs397515529
NM_000500.9(CYP21A2):c.17TGC[6] (p.Leu10dup)	rs61338903
NM_000500.9(CYP21A2):c.552C>G (p.Asp184Glu)	rs397515531
NM_000500.9(CYP21A2):c.844G>C (p.Val282Leu)	rs6471
NM_000500.9(CYP21A2):c.844G>T (p.Val282Leu)	rs6471

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