We then confirmed the independent association of rs76904798 with PD risk from p.G2019S and p.N2081D (Δ p.G2019S Δ p.N2081D, OR: 1.11, 95% CI: 1.07–1.16, P = 1.40e−07) (Table 2; Fig. S8), the PD‐linked LRRK2 coding variants (Δ p.G2019S Δ p.N551K Δ p.R1398H Δ p.M1646T Δ p.N2081D, OR: 1.11, 95% CI: 1.06–1.16, P = 2.144e−06), and all of the relatively rare LRRK2 coding variants examined in this study (Δ p.G2019S Δ p.N551K Δ p.R1398H Δ p.M1646T Δ p.N2081D Δ p.L119P Δ p.I723V Δ p.R1514Q Δ p.P1542S, OR: 1.09, 95% CI: 1.04–1.15, P = 0.0002082) (Fig. 1). Here, LRRK2 is linked to Parkinson disease.