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About the CanRisk Tool
How are rare genetic pathogenic variants in BRCA1, BRCA2, PALB2, ATM, CHEK2 , RAD51C, RAD51D, and BRIP1 used in the CanRisk Tool?
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The CanRisk Tool only considers the effects of truncating variants in ATM and CHEK2. Please see the explanation for this in the Discussion section of
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Genet. Med. 18, 1190–1198 (2016)
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{"serverDuration": 186, "requestCorrelationId": "87740aa0c8a9414b827238537b1729be"}