ClinVar Miner

List of variants reported as likely pathogenic for Familial cancer of breast; Breast-ovarian cancer, familial, susceptibility to, 1; Pancreatic cancer, susceptibility to, 4; Fanconi anemia, complementation group S by Fulgent Genetics, Fulgent Genetics

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_007294.4(BRCA1):c.287A>G (p.Asp96Gly)	rs864622444
NM_007294.4(BRCA1):c.5165C>T (p.Ser1722Phe)	rs80357104

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