The analysis included sequencing and deletion/duplication screening of 10 genes associated with various genetic disorders: ATM, BRCA1, BRCA2, CDKN2A (p14ARF), CDKN2A (p16INK4a), MLH1, MSH2, MSH6, PALB2, PMS2, and STK11. This evidence concerns the gene PMS2 and hereditary disease.