Genetic variants associated with complement factor H (CFH) and AMD susceptibility gene 2 (ARMS2) are well-established risk factors for the development and progression of AMD [16,17,18,19,20,21,22,23,24,25] (single nucleotide polymorphisms that are found on chromosomes 1q31 and 10q26, respectively). This evidence concerns the gene ARMS2 and age-related macular degeneration.