SHBG and deep vein thrombosis: After harmonization of the alleles and effects between the exposure and outcome in primary analyses, there were 148,148,147 SNPs used for causal analyses of SHBG with VTE, PE, and DVT (R2 = 0.062); 138,140,140 SNPs for TT with VTE, PE, and DVT (R2 = 0.027); and 86,89,91 SNPs for BT with VTE, PE, and DVT (R2 = 0.019).