The two AXIN2 SNPs—rsrs3923087 and rs11867417—also showed significant associations with OPMD/OSCC in both the allelic (OR: 0.58, p = 0.03845, 95%CI: 0.344–0.974; and OR: 0.51, p = 0.010, 95%CI: 0.304–0.857, respectively) and recessive models (OR: 0.40, p = 0.04, 95%CI: 0.168–0.975; and OR: 0.35, p = 0.022, 95%CI: 0.141–0.883, respectively). Here, AXIN2 is linked to oculopharyngeal muscular dystrophy.