nominally significantp = 0.0003
Additionally, we identified one variant (rs2588469) that showed genome-wide significant pleiotropic effects (PLEIO p = 1.18 × 10 −8 ), but showed only nominally significant associations with the three disorders investigated (BP: beta = −0.056, p = 0.0003; MDD: OR = 0.98, p = 9.9 × 10 −5 ; SCZ OR = 1.062, p = 0.0008).