ClinVar Miner

List of variants reported as likely pathogenic 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.8488-14A>G	rs1555287728
NM_000059.4(BRCA2):c.8954-15T>G	rs886040948
NM_000059.4(BRCA2):c.9502-28A>G	rs397508059

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