After filtering against common variants (MAF < 0.01), 2 noncoding and 1 synonymous rare mutation potentially associable with parkinsonism were identified: GIGYF2, PARK11 (c.∗2030G > A, rs115669549); VPS35 gene—vacuolar protein sorting 35, PARK17 (c.102 + 33G > A, rs192115886); and FBXO7, PARK15 (c.540A > G, NP_001028196.1:p.Pro101=, rs41311141) (Figs. 3 and 4). The gene discussed is FBXO7; the disease is Parkinson disease.