In this study we observed that the HNF1B SNPs (rs7501939 and rs4430796) identified in PCa GWAS [23, 24] are associated with PCa risk in AAM and that the CTBP2 SNP (rs4962416), also identified in PCa GWAS [23], are associated with PCa risk in EAM. This evidence concerns the gene HNF1B and posterior cortical atrophy.