As shown in Table 2, Tables S3 and S4, deleterious variants within the receptor subtype of Nogo‐associated genes showed a significant association with PD in the sEOPD & FPD cohort (SKAT‐O p = 0.044), suggesting a potential protective effect (95% CI 0.69–0.99). The gene discussed is RTN4; the disease is Parkinson disease.