In addition, the albuminuria-associated rs780093 (82) in the highly polygenic GCKR locus, as well as the eGFR-associated rs4665972 (in SNX17, but in LD with variants mapped to GCKR), rs11864909 (UMOD), rs10206899 (ALMS1P), rs10899482 (GAB2), and rs9607518 (MAFF), are in LD with variants associated with T2D (https://ldlink.nci.nih.gov/?tab=ldtrait ; search for any “diabetes” in GWAS Catalog for variants in LD (R2 ≥ 0.8 in European population), 21 March 2023), providing some evidence of genetic overlap between T2D and eGFR in diabetes. The gene discussed is SNX17; the disease is type 2 diabetes mellitus.