List of variants reported as likely benign for Familial cancer of breast; Breast-ovarian cancer, familial, susceptibility to, 2; Fanconi anemia complementation group D1; Medulloblastoma; Wilms tumor 1; Pancreatic cancer, susceptibility to, 2; Glioma susceptibility 3; Familial prostate cancer by Department of Pathology and Laboratory Medicine, Sinai Health System

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.682-12T>C	rs780608070	0.00001
NM_000059.4(BRCA2):c.9256+13A>G	rs730881597	0.00001
NM_000059.4(BRCA2):c.9257-8C>T	rs11571819	0.00001
NM_000059.4(BRCA2):c.475+8T>C
NM_000059.4(BRCA2):c.8954-12T>G

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