List of variants in gene CYP11B1 reported as benign for chronic primary adrenal insufficiency

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 19

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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	0.65793
NM_000497.4(CYP11B1):c.*1020C>T	rs5017238	0.63333
NM_000497.4(CYP11B1):c.*1852T>G	rs4736312	0.61613
NM_000497.4(CYP11B1):c.*1566G>T	rs1134096	0.61478
NM_000497.4(CYP11B1):c.*1499C>T	rs1134095	0.61442
NM_000497.4(CYP11B1):c.*318A>G	rs5299	0.60710
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.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	0.34289
NM_000497.4(CYP11B1):c.*1288A>G	rs61752809	0.13081
NM_000497.4(CYP11B1):c.*1417G>A	rs61752812	0.11543
NM_000497.4(CYP11B1):c.*923G>C	rs61752805	0.06064
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.239+13C>A	rs6402	0.00870
NM_000497.4(CYP11B1):c.243C>T (p.Tyr81=)	rs9657022	0.00712

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