Since the above sample set has low number of “T” allele, we evaluated all prostate cancer patients (available in cbioportal with exome/genome/SNP array data from multiple studies; see “Methods” section) who showed genetic alterations (copy number alterations or mutations) and no alterations in the PCAT1, PVT1 and MYC genes, irrespective of the ancestry and genotype at rs72725854. The gene discussed is PCAT1; the disease is Familial prostate cancer.