Genetic factors associated with age‐related macular degeneration: identification of a novel <i>PRPH2</i> single nucleotide polymorphism associated with increased risk of the disease

Abstract

Although PRPH2 mutations have been previously implicated in various forms of retinal degeneration, to the best of our knowledge, this study is the first to show that the rs3818086 variant increases the risk for AMD more than two times. Further studies on larger cohorts are required to elucidate how this variant affects protein structure.