List of variants in gene CYP11B1 reported as benign for adrenal cortex disorder

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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: 33

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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.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.*1288A>G	rs61752809	0.13519
NM_000497.4(CYP11B1):c.*1417G>A	rs61752812	0.11851
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.*1871T>A	rs61752818	0.01316
NM_000497.4(CYP11B1):c.*1076C>T	rs61752806	0.01209
NM_000497.4(CYP11B1):c.*193A>T	rs61752798	0.01010
NM_000497.4(CYP11B1):c.*1512G>A	rs61752814	0.00880
NM_000497.4(CYP11B1):c.*1258G>A	rs61752808	0.00878
NM_000497.4(CYP11B1):c.*468C>T	rs114832894	0.00774
NM_000497.4(CYP11B1):c.239+13C>A	rs6402	0.00753
NM_000497.4(CYP11B1):c.243C>T (p.Tyr81=)	rs9657022	0.00726
NM_000497.4(CYP11B1):c.395+9C>T	rs61751140	0.00235
NM_000497.4(CYP11B1):c.*634G>A	rs1137481	0.00126
NM_000497.4(CYP11B1):c.*718T>G	rs189479208	0.00032
NM_000497.4(CYP11B1):c.375C>G (p.His125Gln)	rs201137503	0.00016
NM_000497.4(CYP11B1):c.104T>C (p.Val35Ala)	rs201951316	0.00011
NM_000497.4(CYP11B1):c.395+6C>T	rs553707049	0.00003
NM_000497.4(CYP11B1):c.*1020C>T	rs5017238
NM_000497.4(CYP11B1):c.*193A>C	rs61752798
NM_000497.4(CYP11B1):c.*848C>T	rs149520110

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