The carrier rates of P/LP mutation in the UKB unselected PCa patients (data available in 5896 PCa patients) for each of the ten genes were shown in Table 3, ranging from 0.02% for MLH1 to 1.64% for CHEK2 (Mutations listed in Additional file 1: Table S7). This evidence concerns the gene CHEK2 and posterior cortical atrophy.