Interestingly, our combined analysis identified two novel genome-wide significant associations, the first for SLCO1A2 rs11568563 (OR = 0.67, P = 5.3E-10) and the second for DUSP10 rs6687758 (OR = 0.8, P = 1.14E-8); both of these variants displayed associations with PSP in the previous GWAS that did not quite meet genome-wide significance. The gene discussed is SLCO1A2; the disease is supranuclear palsy, progressive, 1.