Additional file 1 of Genomic architecture of autism spectrum disorder in Qatar: The BARAKA-Qatar Study

Additional file 1: Table S1. Detail phenotypes of individuals with ASD, Table S2. Known ASD/NDD gene panels, Table S3. Known mtDNA pathogenic variants associated with hearing loss/Deafness at greater than 2% heteroplasmy, Table S4. Candidate dominant variants in Novel genes/regions associated with ASD.