List of variants in gene combination HSD3B2, LOC109029530 reported as likely benign for adrenocortical 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000198.4(HSD3B2):c.124T>C (p.Leu42=)	rs370732845	0.00016
NM_000198.4(HSD3B2):c.13T>A (p.Cys5Ser)	rs376207606	0.00005
NM_000198.4(HSD3B2):c.51G>A (p.Arg17=)	rs757957605

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