In a recent PSP GWAS [27], four loci near MAPT, STX6, EIF2AK3, and MOBP conferred significant risk, in addition to three suggestive loci at 1q41 intergenic locus, BMS1 and SLCO1A2. We assessed these seven strongest PSP risk loci in our eGWAS in the ADs, non–ADs and combined datasets, as well as the PSP subset of non–ADs (Table 5, Supplementary Table 16 in Dataset S1). The gene discussed is STX6; the disease is supranuclear palsy, progressive, 1.