Schellenberg et al. showed that EIF2AK3 haplotype B harboring minor alleles of three nonsynonymous single nucleotide variants (SNVs), including rs7571971, in the coding region was associated with increased PSP risk (Hoglinger et al. 2011; Stutzbach et al. 2013). The gene discussed is EIF2AK3; the disease is supranuclear palsy, progressive, 1.