The risk allele diminishes androgen receptor (AR) occupancy, is associated with decreased H3K27ac levels, and downregulates the expression of VPS53, FAM57A, and GEMIN4, and the knockdown of VPS53, FAM57A, and GEMIN4 in prostate cancer cells results in an increase in cell viability [153]. This evidence concerns the gene TLCD3A and prostate cancer.