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Analysis of hereditary cancer gene variant classifications from ClinVar indicates a need for regular reassessment of clinical assertions

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The clinical classification of variants may change with new information, however, there is limited guidance on how often significant changes in variant classification occur. We used ClinVar to examine how… Click to show full abstract

The clinical classification of variants may change with new information, however, there is limited guidance on how often significant changes in variant classification occur. We used ClinVar to examine how variant classification changes over time. We developed a custom parser and accessed variant data from ClinVar between January 2015 and July 2021. The ClinVar‐assigned “aggregate” classification of variants in 121 hereditary cancer genes was harmonized across releases to align to the American College of Medical Genetics and Genomics and the Association for Molecular Pathology terms. Aggregate classification categories were grouped as: benign/likely benign (B/LB); likely pathogenic/pathogenic (LP/P); variant of uncertain significance (VUS); conflicting interpretations of pathogenicity (Conflicting); or Other. We profiled changes in aggregate variant classification between consecutive semi‐annual ClinVar releases. The proportion of variants that changed aggregate classification between semi‐annual ClinVar releases ranged from 0.6% to 6.4%. The most frequent changes were “VUS to conflicting,” “other to LP/P,” and “B/LB to Conflicting.” A limited number of variants changed aggregate classification from “LP/P to B/LB,” or vice versa. Our analysis indicates need for regular reassessment of clinical variant interpretations. The parser developed for this project will facilitate extraction of relevant interpretation data from ClinVar.

Keywords: need regular; clinvar; aggregate classification; classification; hereditary cancer; indicates need

Journal Title: Human Mutation
Year Published: 2022

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