List of variants in gene BRCA2 reported as likely benign by Institute of Human Genetics, University of Leipzig Medical Center

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.4068G>A (p.Leu1356=)	rs28897724	0.00295
NM_000059.4(BRCA2):c.68-7T>A	rs81002830	0.00277
NM_000059.4(BRCA2):c.1792A>G (p.Thr598Ala)	rs28897710	0.00182
NM_000059.4(BRCA2):c.978C>A (p.Ser326Arg)	rs28897706	0.00082
NM_000059.4(BRCA2):c.2779A>G (p.Met927Val)	rs786201837
NM_000059.4(BRCA2):c.317-19_317-12del	rs1555280834

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