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Low-frequency and rare-coding variation contributes to multiple sclerosis risk

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Item Type:Article
Title:Low-frequency and rare-coding variation contributes to multiple sclerosis risk
Creators Name:Cotsapas, C.
Abstract:Multiple sclerosis is a complex neurological disease, with ∼20% of risk heritability attributable to common genetic variants, including >230 identified by genome-wide association studies. Multiple strands of evidence suggest that much of the remaining heritability is also due to additive effects of common variants rather than epistasis between these variants or mutations exclusive to individual families. Here, we show in 68,379 cases and controls that up to 5% of this heritability is explained by low-frequency variation in gene coding sequence. We identify four novel genes driving MS risk independently of common-variant signals, highlighting key pathogenic roles for regulatory T cell homeostasis and regulation, IFNγ biology, and NFκB signaling. As low-frequency variants do not show substantial linkage disequilibrium with other variants, and as coding variants are more interpretable and experimentally tractable than non-coding variation, our discoveries constitute a rich resource for dissecting the pathobiology of MS.
Keywords:Genetic Epistasis, Genetic Predisposition to Disease, Genome-Wide Association Study, Linkage Disequilibrium, Multiple Sclerosis, Mutation, Open Reading Frames, Risk Factors
Source:Cell
ISSN:0092-8674
Publisher:Cell Press
Volume:175
Number:6
Page Range:1679-1687
Date:29 November 2018
Additional Information:Friedemann Paul is a member of the International Multiple Sclerosis Genetics Consortium.
Official Publication:https://doi.org/10.1016/j.cell.2018.09.049
PubMed:View item in PubMed

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