Our analysis also included 3 SNPs related to HRD; RNF8 rs2284922 SNP, found in approximately 44% of the 1000 genome UK population and BARD1’s rs2070096 and rs2229571 SNPs, which occur in approximately 19% and 45% of the 1000 genome population, respectively. Here, RNF8 is linked to hypoparathyroidism-retardation-dysmorphism syndrome.