About the CanRisk Tool
The CanRisk Tool is used to compute breast and ovarian cancer risks and mutation carrier probabilities.
- What does the CanRisk Tool do?
- Can I use the CanRisk Tool to estimate risks for populations outside Europe?
- What web browsers are supported by CanRisk?
- Who can use the CanRisk Tool?
- Why have I not received my account activation email?
- Can the target/proband can be changed?
- What pedigree data management/ drawing programs can export pedigrees to the BOADICEA format?
- What is your policy on software bugs?
- Which paper should I cite when describing results generated with the CanRisk Tool?
- Can automatic synchronisation of the age and year of birth fields be switched off?
- Can I specify default settings for the proband's country of residence and mutation search sensitivities?
- How are rare genetic pathogenic variants in BRCA1, BRCA2, PALB2, ATM, CHEK2 , RAD51C, RAD51D, and BRIP1 used in the CanRisk Tool?
- What rare genetic variants are considered in the breast and ovarian cancer models?
