SH2B3 and coronary artery disorder: In this same population, the allele “T” in SH2B3 rs2078863 was associated with decreased odds of CAD risk in the codominant (p = 0.022), recessive (CC vs. TT + TC: OR = 0.44, 95% CI: 0.24-0.82; p = 0.007), and additive (OR = 0.64, 95% CI: 0.44-0.91; p = 0.012) models.