List of variants in gene combination HSD3B2, LOC109029530 reported by Fulgent Genetics, Fulgent Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 4

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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.15C>A (p.Cys5Ter)	rs766474996	0.00002
NM_000198.4(HSD3B2):c.29C>A (p.Ala10Glu)	rs28934880	0.00001
NM_000198.4(HSD3B2):c.51G>A (p.Arg17=)	rs757957605

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