The phenotypic analysis of 69 compound heterozygous patients with the TYR c.1205G>A, p. (Arg402Gln) variant, displaying ocular features of albinism, revealed predominant traits including blue irises (76.56%), white or yellow-white hair at birth (71.43%), transitioning to blond hair later (46.97%), and generally light skin with residual pigmentation exceeding that typically observed in classical OCA1 cases (69.64%) [31]. This evidence concerns the gene TYR and albinism.