Six independent variants located in or near RND3/RBM43, SLITRK3, ENPP7, GNG7, EFNB2, and APOL1 were associated with T2D-ESKD (p-value < 5 × 10−8), whereby variants in EFNB2, GNG7, and APOL1 were also associated with all-cause ESKD (48). This evidence concerns the gene GNG7 and type 2 diabetes mellitus.