List of variants in gene combination CYP11B1, LOC106799833 reported as benign by Athena Diagnostics Inc

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.1399-14G>C	rs5295	0.12635
NM_000497.4(CYP11B1):c.873G>A (p.Ala291=)	rs34570566	0.08763
NM_000497.4(CYP11B1):c.800-14C>T	rs4535	0.05537
NM_000497.4(CYP11B1):c.1098T>G (p.Arg366=)	rs61752769	0.02016
NM_000497.4(CYP11B1):c.1122-20A>G	rs61752794	0.01661
NM_000497.4(CYP11B1):c.1353T>C (p.Leu451=)	rs5316	0.01232
NM_000497.4(CYP11B1):c.825T>C (p.Tyr275=)	rs5290	0.00338
NM_000497.4(CYP11B1):c.743C>T (p.Thr248Ile)	rs34620645	0.00095
NM_000497.4(CYP11B1):c.459T>C (p.Ala153=)	rs61751150	0.00079
NM_000497.4(CYP11B1):c.1120C>A (p.Arg374=)	rs61752786

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