WNT11 rs1533767 was significantly associated with OPMD/OSCC in the genotypic model (p = 0.038), as well as in the allelic (OR: 1.94, p = 0.042, 95% CI: 1.018–3.694) and dominant models (OR: 1.94, p = 0.042, 95%CI: 1.018–3.694). The gene discussed is WNT11; the disease is oculopharyngeal muscular dystrophy.