AUTHOR=Read Robert W. , Schlauch Karen A. , Lombardi Vincent C. , Cirulli Elizabeth T. , Washington Nicole L. , Lu James T. , Grzymski Joseph J. TITLE=Genome-Wide Identification of Rare and Common Variants Driving Triglyceride Levels in a Nevada Population JOURNAL=Frontiers in Genetics VOLUME=12 YEAR=2021 URL=https://www.frontiersin.org/journals/genetics/articles/10.3389/fgene.2021.639418 DOI=10.3389/fgene.2021.639418 ISSN=1664-8021 ABSTRACT=
Clinical conditions correlated with elevated triglyceride levels are well-known: coronary heart disease, hypertension, and diabetes. Underlying genetic and phenotypic mechanisms are not fully understood, partially due to lack of coordinated genotypic-phenotypic data. Here we use a subset of the Healthy Nevada Project, a population of 9,183 sequenced participants with longitudinal electronic health records to examine consequences of altered triglyceride levels. Specifically, Healthy Nevada Project participants sequenced by the Helix Exome+ platform were cross-referenced to their electronic medical records to identify: (1) rare and common single-variant genome-wide associations; (2) gene-based associations using a Sequence Kernel Association Test; (3) phenome-wide associations with triglyceride levels; and (4) pleiotropic variants linked to triglyceride levels. The study identified 549 significant single-variant associations (