List of variants in gene BRCA2 reported as likely benign by Genome Diagnostics Laboratory, Amsterdam University 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.1040A>G (p.Gln347Arg)	rs55800493	0.00109
NM_000059.4(BRCA2):c.1911T>C (p.Gly637=)	rs11571652	0.00109
NM_000059.4(BRCA2):c.4584C>T (p.Ser1528=)	rs80359788	0.00026

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