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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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{"serverDuration": 146, "requestCorrelationId": "9cf21b01209b499aa9e4eef749b51b04"}