We evaluated the association of the RETN and IL1RL1 SNPs with resistin and sST2 levels in the patients with CAD (Table 1), and the results revealed significant associations, except for rs370006313 genotypes for resistin levels (rs3219175, rs370006313, and rs3745368 genotypes for resistin levels, p = 4.89 × 10−15, p = 0.055, and p = 0.001, respectively, and rs10183388 and rs4142132 genotypes for sST2 levels, p = 4.49 × 10−8 and p = 8.00 × 10−6, respectively). Here, RETN is linked to coronary artery disorder.