In the Uygur Chinese population, variant rs9902941 of SREBP-1 exhibited significant differences between the CAD and control groups in a recessive model (TT vs. CT + CC, P = 0.032), nevertheless, the difference was no longer significant after Bonferroni's correction (P > 0.05/3 = 0.0167). The gene discussed is SREBF1; the disease is coronary artery disorder.