List of variants in gene BRCA2 reported as pathogenic for Familial prostate cancer

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.1238del (p.Leu413fs)	rs80359271
NM_000059.4(BRCA2):c.2516dup (p.Tyr839Ter)	rs1593897122
NM_000059.4(BRCA2):c.3202_3203del (p.Val1068fs)
NM_000059.4(BRCA2):c.3641dup (p.Phe1216fs)	rs397507678
NM_000059.4(BRCA2):c.4889C>A (p.Ser1630Ter)	rs80358711
NM_000059.4(BRCA2):c.5734G>T (p.Glu1912Ter)	rs397507800
NM_000059.4(BRCA2):c.7673_7674del (p.Glu2558fs)	rs80359672
NM_000059.4(BRCA2):c.7977-1G>C	rs81002874

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