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Abstract
The impact of the parental origin of associated alleles in GWAS has been largely ignored. Yet sequence variants could affect traits differently depending on whether they are inherited from the mother or the father, as in imprinted regions, where identical inherited DNA sequences can have different effects based on the parental origin. To explore parent-of-origin effects (POEs), we studied 21 quantitative phenotypes in a large Hutterite pedigree to identify variants with single parent (maternal-only or paternal-only) effects, and then variants with opposite parental effects. Here we show that POEs, which can be opposite in direction, are relatively common in humans, have potentially important clinical effects, and will be missed in traditional GWAS. We identified POEs with 11 phenotypes, most of which are risk factors for cardiovascular disease. Many of the loci identified are characteristic of imprinted regions and are associated with the expression of nearby genes.
Sahar Mozaffari et al. conduct a parent of origin genome-wide association study in a large Hutterite pedigree to determine parent-of-origin effects on 21 phenotypes. They identify effects on 11 phenotypes (including single parent and opposite parental effects), most of which are associated with cardiovascular disease.
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1 University of Chicago, Department of Human Genetics, Chicago, USA (GRID:grid.170205.1) (ISNI:0000 0004 1936 7822); University of Chicago, Committee on Genetics, Genomics, and Systems Biology, Chicago, USA (GRID:grid.170205.1) (ISNI:0000 0004 1936 7822)
2 University of Chicago, Department of Medicine, Chicago, USA (GRID:grid.170205.1) (ISNI:0000 0004 1936 7822)
3 Northwestern University Feinberg School of Medicine, Department of Medicine, Chicago, USA (GRID:grid.16753.36) (ISNI:0000 0001 2299 3507)
4 Istituto di Ricerca Genetica e Biomedica (IRGB), CNR, Monserrato, Italy (GRID:grid.428485.7) (ISNI:0000 0004 1789 9390)
5 Istituto di Ricerca Genetica e Biomedica (IRGB), CNR, Monserrato, Italy (GRID:grid.428485.7) (ISNI:0000 0004 1789 9390); Universita di Sassari, Dipartimento di Scienze Biomediche, Sassari, Italy (GRID:grid.11450.31) (ISNI:0000 0001 2097 9138)
6 University of Chicago, Department of Human Genetics, Chicago, USA (GRID:grid.170205.1) (ISNI:0000 0004 1936 7822); University of Chicago, Committee on Genetics, Genomics, and Systems Biology, Chicago, USA (GRID:grid.170205.1) (ISNI:0000 0004 1936 7822); University of Chicago, Department of Medicine, Chicago, USA (GRID:grid.170205.1) (ISNI:0000 0004 1936 7822); University of Chicago, Department of Statistics, Chicago, USA (GRID:grid.170205.1) (ISNI:0000 0004 1936 7822)