With the exception of four cases, all others were previously investigated for BRCA1 and BRCA2 pathogenic variants, and were negative for pathogenic/likely pathogenic BRCA1/BRCA2 variants We used targeted next-generation sequencing of a multigene panel, comprised of 94 cancer susceptibility genes (Illumina TruSight cancer panel) in order to assess the frequency of deleterious germline variants in this cohort. This evidence concerns the gene BRCA2 and cancer.