List of variants in gene CYP11A1 reported as likely benign by GeneDx

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000781.3(CYP11A1):c.991-149G>A	rs72547454	0.01680
NM_000781.3(CYP11A1):c.426-47G>A	rs117641050	0.01263
NM_000781.3(CYP11A1):c.939C>T (p.Phe313=)	rs4986873	0.01114
NM_000781.3(CYP11A1):c.535G>A (p.Val179Ile)	rs58174009	0.00415
NM_000781.3(CYP11A1):c.830-125G>T	rs79533289

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