GBA1 p.Leu483Pro is among the three most common variants in patients with PD (Guadagnolo et al., 2021; Huang et al., 2011; J. L. Lim et al., 2022; Petrucci et al., 2020; Ren et al., 2022; Wu et al., 2007), whereas the splice‐site variant g.9069G>A (c.115+1G>A) has previously been identified in both PD subjects and asymptomatic carriers (Aslam et al., 2021; Sato et al., 2005). The gene discussed is GBA1; the disease is Parkinson disease.