SMARCC2 and Behcet disease: We also found enrichment of LoF gDNMs in SMARCC2, encoding a component of the SWI/SNF chromatin remodeling complexes, with significance close to the exome-wide threshold in the combined group of BD, schizophrenia, and ASD (P = 5.62 × 10−6, one-tailed Poisson test).