The most robust associations found for each phenotype are as follows: DMFT with rs79198416 (near CDC73/KCNT2; p = 7.57E-07), periodontal disease with rs73870587 (DIPK2A, p = 7.38E-08); CIMT with rs113152669 (LRP1Bp = 4.07E-07), and CAC with rs76676138 (CNTNAP2; p = 2.47E-19). The gene discussed is DIPK2A; the disease is periodontal disorder.