Literature DB >> 24357849

Large numbers of individuals are required to classify and define risk for rare variants in known cancer risk genes.

Brian H Shirts1, Angela Jacobson1, Gail P Jarvik2, Brian L Browning3.   

Abstract

PURPOSE: Up to half of unique genetic variants in genomic evaluations of familial cancer risk will be rare variants of uncertain significance. Classification of rare variants will be an ongoing issue as genomic testing becomes more common.
METHODS: We modified standard power calculations to explore sample sizes necessary to classify and estimate relative disease risk for rare variant frequencies (0.001-0.00001) and varying relative risk (20-1.5), using population-based and family-based designs focusing on breast and colon cancer. We required 80% power and tolerated a 10% false-positive rate because variants tested will be in known genes with high pretest probability.
RESULTS: Using population-based strategies, hundreds to millions of cases are necessary to classify rare cancer variants. Larger samples are necessary for less frequent and less penetrant variants. Family-based strategies are robust to changes in variant frequency and require between 8 and 1,175 individuals, depending on risk.
CONCLUSION: It is unlikely that most rare missense variants will be classifiable in the near future, and accurate relative risk estimates may never be available for very rare variants. This knowledge may alter strategies for communicating information about variants of uncertain significance to patients.

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Year:  2013        PMID: 24357849      PMCID: PMC4063879          DOI: 10.1038/gim.2013.187

Source DB:  PubMed          Journal:  Genet Med        ISSN: 1098-3600            Impact factor:   8.822


  35 in total

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4.  Actionable, pathogenic incidental findings in 1,000 participants' exomes.

Authors:  Michael O Dorschner; Laura M Amendola; Emily H Turner; Peggy D Robertson; Brian H Shirts; Carlos J Gallego; Robin L Bennett; Kelly L Jones; Mari J Tokita; James T Bennett; Jerry H Kim; Elisabeth A Rosenthal; Daniel S Kim; Holly K Tabor; Michael J Bamshad; Arno G Motulsky; C Ronald Scott; Colin C Pritchard; Tom Walsh; Wylie Burke; Wendy H Raskind; Peter Byers; Fuki M Hisama; Deborah A Nickerson; Gail P Jarvik
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Review 10.  Mutations associated with HNPCC predisposition -- Update of ICG-HNPCC/INSiGHT mutation database.

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Review 3.  Family-Specific Variants and the Limits of Human Genetics.

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9.  Power to the People: Data Citizens in the Age of Precision Medicine.

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10.  The challenge of comprehensive and consistent sequence variant interpretation between clinical laboratories.

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