Gene‐based burden analysis showed nominal associations with PD risk for coding (n = 33; SKAT P = 0.023, SKAT‐O P = 0.022) and missense variants (n = 18; SKAT P = 0.022, SKAT‐O P = 0.019) in the GP2 EUR group. The gene discussed is GP2; the disease is Parkinson disease.