| Literature DB >> 31427789 |
Kyoko Watanabe1, Sven Stringer1, Oleksandr Frei2, Maša Umićević Mirkov1, Christiaan de Leeuw1, Tinca J C Polderman1, Sophie van der Sluis1,3, Ole A Andreassen2,4, Benjamin M Neale5,6,7, Danielle Posthuma8,9.
Abstract
After a decade of genome-wide association studies (GWASs), fundamental questions in human genetics, such as the extent of pleiotropy across the genome and variation in genetic architecture across traits, are still unanswered. The current availability of hundreds of GWASs provides a unique opportunity to address these questions. We systematically analyzed 4,155 publicly available GWASs. For a subset of well-powered GWASs on 558 traits, we provide an extensive overview of pleiotropy and genetic architecture. We show that trait-associated loci cover more than half of the genome, and 90% of these overlap with loci from multiple traits. We find that potential causal variants are enriched in coding and flanking regions, as well as in regulatory elements, and show variation in polygenicity and discoverability of traits. Our results provide insights into how genetic variation contributes to trait variation. All GWAS results can be queried and visualized at the GWAS ATLAS resource ( https://atlas.ctglab.nl ).Entities:
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Year: 2019 PMID: 31427789 DOI: 10.1038/s41588-019-0481-0
Source DB: PubMed Journal: Nat Genet ISSN: 1061-4036 Impact factor: 38.330