FBXO7 and Parkinson disease: After filtering against common variants (minor allele frequency (MAF) < 0.01), 2 noncoding and 1 synonymous rare mutation potentially associable with parkinsonism were identified: GIGYF2—GRB10 Interacting GYF Protein 2, PARK11 (c.∗2030G > A, rs115669549); VPS35 gene—vacuolar protein sorting 35, PARK17 (c.102 + 33G > A, rs192115886); and FBXO7—F-box only protein 7 gene, PARK15 (c.540A > G, rs41311141).