Variant curation and interpretation in hereditary cancer genes: An institutional experience in Latin America
ConclusionsMost VUS were reclassified as benign/likely benign. Since false-positive and -negative results can be obtained with automated tools, manual curation should also be used as a complement. Our results contribute to improving cancer risk assessment and management for a broad range of hereditary cancer syndromes in Hispanic/Latino populations.
Source: Molecular Genetics & Genomic Medicine - Category: Genetics & Stem Cells Authors: Mar ía Carolina Manotas,
Ana Lucia Rivera,
María Carolina Sanabria‐Salas Tags: ORIGINAL ARTICLE Source Type: research