The variants rs12118522 (p-value = 4.52 x  10−08) and rs115505361 (p-value = 4.49 x 10−08) were associated with TG, mapped within CHRM3 and MGAT2, and associated with hypertension, body fat distribution and body mass index and blood protein levels, respectively, Fig. 2. The gene discussed is MGAT2; the disease is hypertensive disorder.