List of variants in gene BRCA2 reported as likely benign by ClinGen ENIGMA BRCA1 and BRCA2 Variant Curation Expert Panel, ClinGen

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.663T>G (p.Phe221Leu)	rs80358891	0.00003
NM_000059.4(BRCA2):c.2471T>C (p.Leu824Ser)	rs397507631	0.00001
NM_000059.4(BRCA2):c.2482T>C (p.Tyr828His)	rs1060502466	0.00001
NM_000059.4(BRCA2):c.5629AAC[1] (p.Asn1878del)	rs794727015
NM_000059.4(BRCA2):c.7008-5T>C	rs397507380

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