Furthermore, 14 variants were exclusively identified in the SAS population, with allele frequencies ranging from 1.29 × 10−4 to 1.10 × 10−5, across PLA2G6, GBA1, PINK1, PSAP, PRKN, FBXO7, and ATP13A2. The gene discussed is GBA1; the disease is SATB2 associated disorder.