List of variants studied for Familial cancer of breast; Breast-ovarian cancer, familial, susceptibility to, 2; Fanconi anemia complementation group D1; Medulloblastoma; Wilms tumor 1; Malignant tumor of prostate; Pancreatic cancer, susceptibility to, 2; Glioma susceptibility 3; Tracheoesophageal fistula

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.7051G>A (p.Ala2351Thr)	rs80358930	0.00006
NM_000059.4(BRCA2):c.5857G>T (p.Glu1953Ter)	rs80358814	0.00001
NM_000059.4(BRCA2):c.9117G>A (p.Pro3039=)	rs28897756	0.00001
NM_000059.4(BRCA2):c.145G>T (p.Glu49Ter)	rs80358435
NM_000059.4(BRCA2):c.5682C>G (p.Tyr1894Ter)	rs41293497
NM_000059.4(BRCA2):c.7625C>T (p.Thr2542Met)	rs80358989

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