Phenome-wide heritability analysis of the UK Biobank.

PLoS Genet
Authors
Keywords
Abstract

Heritability estimation provides important information about the relative contribution of genetic and environmental factors to phenotypic variation, and provides an upper bound for the utility of genetic risk prediction models. Recent technological and statistical advances have enabled the estimation of additive heritability attributable to common genetic variants (SNP heritability) across a broad phenotypic spectrum. Here, we present a computationally and memory efficient heritability estimation method that can handle large sample sizes, and report the SNP heritability for 551 complex traits derived from the interim data release (152,736 subjects) of the large-scale, population-based UK Biobank, comprising both quantitative phenotypes and disease codes. We demonstrate that common genetic variation contributes to a broad array of quantitative traits and human diseases in the UK population, and identify phenotypes whose heritability is moderated by age (e.g., a majority of physical measures including height and body mass index), sex (e.g., blood pressure related traits) and socioeconomic status (education). Our study represents the first comprehensive phenome-wide heritability analysis in the UK Biobank, and underscores the importance of considering population characteristics in interpreting heritability.

Year of Publication
2017
Journal
PLoS Genet
Volume
13
Issue
4
Pages
e1006711
Date Published
2017 Apr
ISSN
1553-7404
DOI
10.1371/journal.pgen.1006711
PubMed ID
28388634
PubMed Central ID
PMC5400281
Links
Grant list
K24 MH094614 / MH / NIMH NIH HHS / United States
MC_QA137853 / Medical Research Council / United Kingdom