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CanRisk v2.4.0 - updated BRCA2 relative risks
CanRisk v2.4.0 - updated BRCA2 relative risks
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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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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 are BRCA1 and BRCA2 mutations defined?
How are BRCA1 and BRCA2 mutations defined?
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Can the CanRisk Tool estimate risks for Ashkenazi Jewish individuals?
Can the CanRisk Tool estimate risks for Ashkenazi Jewish individuals?
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Why do BRCA mutation carrier probabilities sometimes increase abruptly when I increase an age at breast cancer diagnosis from 19 to 20 years in my input pedigree?
Why do BRCA mutation carrier probabilities sometimes increase abruptly when I increase an age at breast cancer diagnosis from 19 to 20 years in my input pedigree?
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About CanRisk Web-Services
About CanRisk Web-Services
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