List of variants in gene CYP11B1 reported as likely benign for Deficiency of steroid 11-beta-monooxygenase

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_000497.4(CYP11B1):c.*1871T>A	rs61752818	0.01230
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.243C>T (p.Tyr81=)	rs9657022	0.00712
NM_000497.4(CYP11B1):c.*634G>A	rs1137481	0.00194
NM_000497.4(CYP11B1):c.*718T>G	rs189479208	0.00101
NM_000497.4(CYP11B1):c.*193A>C	rs61752798

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