Autism spectrum disorder trios from consanguineous populations are enriched for rare biallelic variants, identifying 32 new candidate genes

BackgroundAutism spectrum disorder (ASD) is a neurodevelopmental disorder that affects about 1 in 36 children in the United States, imposing enormous economic and socioemotional burden on families and communities. Genetic studies of ASD have identified de novo copy number variants (CNVs) and point mutations that contribute significantly to the genetic architecture, but the majority of these studies were conducted in populations unsuited for detecting autosomal recessive (AR) inheritance. However, several ASD studies in consanguineous populations point towards AR as an under-appreciated source of ASD variants. MethodsWe used whole exome sequencing to look for rare variants for ASD in 115 proband-mother-father trios from populations with high rates of consanguinity, namely Pakistan, Iran, and Saudi Arabia. Consanguinity was assessed through microarray genotyping. ResultsWe report 84 candidate disease-predisposing single nucleotide variants and indels, with 58% biallelic, 25% autosomal dominant/de novo, and the rest X-linked, in 39 trios. 52% of the variants were loss of function (LoF) or putative LoF (pLoF), and 47% nonsynonymous. We found an enrichment of biallelic variants, both in sixteen genes previously reported for AR ASD and/or intellectual disability (ID) and 32 previously unreported AR candidate genes (including DAGLA, ENPP6, FAXDC2, ILDR2, KSR2, PKD1L1, SCN10A, SHH, and SLC36A1). We also identified eight candidate biallelic exonic loss CNVs. ConclusionsThe significant enrichment for biallelic variants among individuals with high Froh coefficients, compared with low Froh, either in known or candidate AR genes, confirms that genetic architecture for ASD among consanguineous populations is different to non-consanguineous populations. Assessment of consanguinity may assist in the genetic diagnostic process for ASD.