These are chiefly focused on the FSGS/Nephrotic syndrome spectrum and were strongly represented in the data set, covering about 60-65% of OMIM-mentioned FSGS-associated genes, followed by genes responsible for ciliopathies (nephronophthisis, Joubert, Bardet-Biedel Syndrome), and autosomal dominant polycystic kidney disease (ADPKD) and autosomal recessive polycystic kidney disease (ARPKD), namely GANAB3 and PKHD1 in addition to PKD1, PKD226,46. Here, PKD1 is linked to autosomal dominant polycystic kidney disease.