Secondly, the variant (rs1800553) from UAE S014 was described by ClinVar as “age-related macular degeneration 2, susceptibility to retinal dystrophy, inborn genetic diseases, cone rod dystrophy 3, ABCA4 Related Disorders” and has a UAE allele frequency as high as 1.9% (see Supplementary Table S17). The gene discussed is ABCA4; the disease is hereditary disease.