Afshari et al. [40] also applied GWAS on 1404 FECD cases and 2564 controls of European ancestry and reported additional three novel loci KANK4 (rs79742895), LAMC1 (rs3768617), and LINC00970/ATP1B1 (rs1200114) [40]. The gene discussed is ATP1B1; the disease is Fuchs endothelial corneal dystrophy.