miR-21, miR-184, miR-let-7-5p, miR-412-3p, miR-512-3p, miR-302-3p, miR-517-3p, miR-30c-5p, miR-SAT, miR-OAZ, miR-H3F3A, and miR-24-3p have all shown significant differences in patients with OSCC and/or an OPMD compared to control groups [44,45,46,47,48,49]. The gene discussed is SAT1; the disease is oculopharyngeal muscular dystrophy.