The study also included the rs147546939 c.1185-6208A>G variant, located in intron 3 of the TYR gene, which has been associated with albinism in European patients as part of the haplotype [c.575C>A p.(Ser192Tyr); c.1185-6208A>G; c.1205G>A p.(Arg402Gln)] (rs1042602A–rs147546939G–rs1126809A) [18]. Here, TYR is linked to albinism.