In addition to NGFR, the expression of a number of SZ, BD and ASD candidate was significantly affected by HS, including SMARCA2, HIST1H2BD, DPP10, SLC6A8, SLC17A7, ARNT2, AHI1 and ZNF804A. SMARCA2, which increased 1.7 fold with HS, encodes a REST-regulated, SWI/SNF chromatin-remodeling complex that has been implicated in SZ in a low density GWAS and CNV screening, and by molecular analysis following REST knockdown [46], [107], [108]. The gene discussed is SLC6A8; the disease is Behcet disease.