List of variants in gene BRCA2 reported as benign for Breast carcinoma

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.1114A>C (p.Asn372His)	rs144848	0.23116
NM_000059.4(BRCA2):c.2971A>G (p.Asn991Asp)	rs1799944	0.04357
NM_000059.4(BRCA2):c.865A>C (p.Asn289His)	rs766173	0.03693

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