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What does the CanRisk Tool do?

What does the CanRisk Tool do?


The CanRisk Tool calculates the risks of breast and ovarian cancer in women based on their risk factors (e.g. lifestyle, hormonal), genetic test results and family history. It also calculates the probability that they are carriers of any cancer-associated mutations in the BRCA1, BRCA2, PALB2, CHEK2, ATM, RAD51D, RAD51C, BARD1 or BRIP1 gene.



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About the CanRisk Tool
About the CanRisk Tool
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How are rare genetic pathogenic variants in BRCA1, BRCA2, PALB2, ATM, CHEK2 , RAD51C, RAD51D, and BRIP1 used in 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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Mutation carrier probabilities in families with members that have two or more mutations or families with mutations in more than one gene
Mutation carrier probabilities in families with members that have two or more mutations or families with mutations in more than one gene
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Why has the CanRisk Tool calculated mutation carrier probabilities but not cancer risks?
Why has the CanRisk Tool calculated mutation carrier probabilities but not cancer risks?
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How-To Use CanRisk Web-Services
How-To Use CanRisk Web-Services
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Can the CanRisk Tool be used to estimate breast cancer risks for both breasts after a patient has developed a first breast cancer? 
Can the CanRisk Tool be used to estimate breast cancer risks for both breasts after a patient has developed a first breast cancer? 
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