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This document discusses analyzing sequence variants of unknown clinical significance in the BRCA1 and BRCA2 genes. It presents the results of analyzing variants found in healthy Croatian individuals. 9 novel variants were identified, including intronic, synonymous, missense, and deletion variants. Accurately assessing the clinical significance of unclassified variants requires considering factors like the type of mutation, location in the gene, presence in control populations, co-segregation with disease, a

Author

02213

Language

EN