“…Although it is a candidate gene study, we used an SNP tagging approach which reduces the bias inherit to the selection of well published SNPs and allows the inclusion of novel genetic variants with possible new biological roles. The phenomenon was previously observed in our series 23,24 , a fact explained by differences in the natural history of the populations 32,33 . As expected, the Andalusian population showed significant differences in genotype and allelic distribution, and subsequently, this subset of PCa patients was excluded from the association analyses to avoid the intra-ethnic bias.…”