SH3GL2 and Parkinson disease: Furthermore, 6 out of 49 variants were present in multiple PD cases and located in five genes (DNAH1: c.10915G>A: p.A3639T (NM_015512), STAB1: c.3265A>G: p.S1089G (NM_015136), ANK2: c.10901T>A: p.V3634D (NM_001148), ANK2: c.11716C>T: p.R3906W (NM_001148), SH3GL2: c.827G>T: p.G276V (NM_003026), NOD2: c.2722G>C: p.G908R (NM_022162) (Table 1).