Three SNPs, two located within CGAS, rs72960018 (OR: 1.68, 95% CI: 1.11‐2.53, P‐value = .01, under dominant model) and rs9352000 (OR: 2.02, 95% CI: 1.07‐3.84, P‐value = .03, under recessive model), and one within TMEM173, rs13153461 (OR: 1.53, 95% CI: 1.03‐2.27, P‐value = .03, under recessive model), exhibited moderate associations with CRC risk (Table 2). The gene discussed is STING1; the disease is colorectal carcinoma.