List of variants in gene BRCA2 reported as likely pathogenic for not specified

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.5511dup (p.Glu1838Ter)	rs2137518141
NM_000059.4(BRCA2):c.7292dup (p.Asn2431fs)	rs2137557686
NM_000059.4(BRCA2):c.7701T>G (p.Tyr2567Ter)	rs1555286423
NM_000059.4(BRCA2):c.8463del (p.Ile2822fs)	rs397507988
NM_000059.4(BRCA2):c.8755-1G>A	rs81002812

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