List of variants reported as likely pathogenic for BRCA2-related cancer predisposition by All of Us Research Program, National Institutes of Health

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Total variants: 8

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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.8063T>C (p.Leu2688Pro)	rs80359045	0.00001
NM_000059.4(BRCA2):c.8177A>G (p.Tyr2726Cys)	rs80359064	0.00001
NM_000059.4(BRCA2):c.9672dup (p.Tyr3225fs)	rs80359773	0.00001
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.8486A>G (p.Gln2829Arg)	rs80359100

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