List of variants reported as likely pathogenic for BRCA2-related cancer predisposition

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Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.9302T>G (p.Leu3101Arg)	rs28897758	0.00005
NM_000059.4(BRCA2):c.632-3C>G	rs568027879	0.00001
NM_000059.4(BRCA2):c.8063T>C (p.Leu2688Pro)	rs80359045	0.00001
NM_000059.4(BRCA2):c.8177A>G (p.Tyr2726Cys)	rs80359064	0.00001
NM_000059.4(BRCA2):c.8350C>T (p.Arg2784Trp)	rs80359075	0.00001
NM_000059.4(BRCA2):c.8524C>T (p.Arg2842Cys)	rs80359104	0.00001
NM_000059.4(BRCA2):c.9672dup (p.Tyr3225fs)	rs80359773	0.00001
NM_000059.4(BRCA2):c.-39-1G>A	rs1060499566
NM_000059.4(BRCA2):c.-39-89del
NM_000059.4(BRCA2):c.-40+1G>A	rs2072249096
NM_000059.4(BRCA2):c.476-4_476-1delinsT	rs587782880
NM_000059.4(BRCA2):c.681+2dup	rs587781486
NM_000059.4(BRCA2):c.6938-2A>G	rs81002863
NM_000059.4(BRCA2):c.7857G>C (p.Trp2619Cys)	rs80359011
NM_000059.4(BRCA2):c.8331G>A (p.Lys2777=)	rs80359802
NM_000059.4(BRCA2):c.8486A>G (p.Gln2829Arg)	rs80359100
NM_000059.4(BRCA2):c.9699_9702del (p.Cys3233fs)	rs80359775

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