List of variants reported as benign for Deficiency of steroid 11-beta-monooxygenase

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Total variants: 27

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HGVS	dbSNP	gnomAD frequency
NM_000497.4(CYP11B1):c.*471A>C	rs12543598	0.67053
NM_000497.4(CYP11B1):c.*694T>C	rs5303	0.65382
NM_000497.4(CYP11B1):c.*1852T>G	rs4736312	0.61613
NM_000497.4(CYP11B1):c.*1566G>T	rs1134096	0.60736
NM_000497.4(CYP11B1):c.*318A>G	rs5299	0.60710
NM_000497.4(CYP11B1):c.*1499C>T	rs1134095	0.60702
NM_000497.4(CYP11B1):c.*738G>A	rs5304	0.60698
NM_000497.4(CYP11B1):c.*1042A>G	rs7003319	0.60695
NM_000497.4(CYP11B1):c.800-45C>T	rs7822986	0.59689
NM_000497.4(CYP11B1):c.225A>G (p.Leu75=)	rs6410	0.52490
NM_000497.4(CYP11B1):c.*516A>G	rs5301	0.49013
NM_000497.4(CYP11B1):c.246C>T (p.Asp82=)	rs5283	0.33818
NM_000497.4(CYP11B1):c.596-41C>T	rs113759408	0.14096
NM_000497.4(CYP11B1):c.*132T>C	rs5297	0.13529
NM_000497.4(CYP11B1):c.*1288A>G	rs61752809	0.13519
NM_000497.4(CYP11B1):c.1399-14G>C	rs5295	0.12635
NM_000497.4(CYP11B1):c.*1417G>A	rs61752812	0.11851
NM_000497.4(CYP11B1):c.873G>A (p.Ala291=)	rs34570566	0.08763
NM_000497.4(CYP11B1):c.*923G>C	rs61752805	0.06064
NM_000497.4(CYP11B1):c.800-14C>T	rs4535	0.05537
NM_000497.4(CYP11B1):c.1157C>T (p.Ala386Val)	rs4541	0.04552
NM_000497.4(CYP11B1):c.128G>A (p.Arg43Gln)	rs4534	0.03864
NM_000497.4(CYP11B1):c.239+20T>A	rs6388	0.03859
NM_000497.4(CYP11B1):c.1086G>C (p.Leu362=)	rs6403	0.03563
NM_000497.4(CYP11B1):c.239+13C>A	rs6402	0.00753
NM_000497.4(CYP11B1):c.*1020C>T	rs5017238
NM_000497.4(CYP11B1):c.595+12G>A	rs6387

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