Mutations in the genes coding α-Synuclein (SNCA), Leucine-rich repeat kinase 2 (LRRK2), vacuolar protein sorting-associated protein 35 (VPS35), parkin RBR E3 ubiquitin-protein ligase (PRKN), PTEN-induced putative kinase 1 (PINK1), glucocerebrosidase (GBA) and oncogene DJ-1 [77] have mostly been found before the onset of genome-wide association studies, while many candidate genes found after are yet to be definitively proven to cause a significant risk for PD. The gene discussed is PINK1; the disease is Parkinson disease.