A genome-wide scan for common alleles affecting risk for autism
Abstract
Although autism spectrum disorders (ASDs) have a substantial genetic basis, most of the known genetic risk has been traced to rare variants, principally copy number variants (CNVs). To identify common risk variation, the Autism Genome Project (AGP) Consortium genotyped 1558 rigorously defined ASD families for 1 million single-nucleotide polymorphisms (SNPs) and analyzed these SNP genotypes for association with ASD. In one of four primary association analyses, the association signal for marker rs4141463, located within MACROD2, crossed the genome-wide association significance threshold of P < 5 × 10(-8). When a smaller replication sample was analyzed, the risk allele at rs4141463 was again over-transmitted; yet, consistent with the winner's curse, its effect size in the replication sample was much smaller; and, for the combined samples, the association signal barely fell below the P < 5 × 10(-8) threshold. Exploratory analyses of phenotypic subtypes yielded no significant associations after correction for multiple testing. They did, however, yield strong signals within several genes, KIAA0564, PLD5, POU6F2, ST8SIA2 and TAF1C.
MeSH terms
Funding
- Autism Speaks
- GlaxoSmithKline
- Johns Hopkins University
- Ontario Innovation Trust
- Genome Canada
- Wellcome Trust
- Health Research Board
- Ontario Genomics
- Hussman Foundation
- Fondation FondaMental
- Fondation Orange
- Ontario Genomics Institute
- Sick Kids Foundation
- Deutsche Forschungsgemeinschaft
- Institut National de la Santé et de la Recherche Médicale
- Koninklijke Nederlandse Akademie van Wetenschappen
- Ministero della Salute
- University of Toronto
- Fondation de France
- Hospital for Sick Children
- National Institutes of Health
- Canadian Institutes of Health Research
- Medical Research Council
- Ontario Ministry of Research and Innovation
- National Institute on Alcohol Abuse and Alcoholism
- National Institute on Drug Abuse
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