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Genome-wide association meta-analysis of 30,000 samples identifies seven novel loci for quantitative ECG traits

Genome-wide association meta-analysis of 30,000 samples identifies seven novel loci for quantitative ECG traits


Title: Genome-wide association meta-analysis of 30,000 samples identifies seven novel loci for quantitative ECG traits
Author: van Setten, Jessica
Verweij, Niek
Mbarek, Hamdi
Niemeijer, Maartje N.
Trompet, Stella
Arking, Dan E.
Brody, Jennifer A.
Gandin, Ilaria
Grarup, Niels
Hall, Leanne M.
... 51 more authors Show all authors
Date: 2019-01-24
Language: English
Scope: 952-962
University/Institute: Háskóli Íslands
University of Iceland
School: Heilbrigðisvísindasvið (HÍ)
School of Health Sciences (UI)
Department: Læknadeild (HÍ)
Faculty of Medicine (UI)
Series: European Journal of Human Genetics;27(6)
ISSN: 1018-4813
1476-5438 (eISSN)
DOI: 10.1038/s41431-018-0295-z
Subject: Genome-wide association studies; Quantitative trait; Erfðarannsóknir; DNA-rannsóknir
URI: https://hdl.handle.net/20.500.11815/1739

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Citation:

van Setten, J., Verweij, N., Mbarek, H. et al. Genome-wide association meta-analysis of 30,000 samples identifies seven novel loci for quantitative ECG traits. European Journal of Human Genetics 27, 952–962 (2019). https://doi.org/10.1038/s41431-018-0295-z

Abstract:

Genome-wide association studies (GWAS) of quantitative electrocardiographic (ECG) traits in large consortia have identified more than 130 loci associated with QT interval, QRS duration, PR interval, and heart rate (RR interval). In the current study, we meta-analyzed genome-wide association results from 30,000 mostly Dutch samples on four ECG traits: PR interval, QRS duration, QT interval, and RR interval. SNP genotype data was imputed using the Genome of the Netherlands reference panel encompassing 19 million SNPs, including millions of rare SNPs (minor allele frequency < 5%). In addition to many known loci, we identified seven novel locus-trait associations: KCND3, NR3C1, and PLN for PR interval, KCNE1, SGIP1, and NFKB1 for QT interval, and ATP2A2 for QRS duration, of which six were successfully replicated. At these seven loci, we performed conditional analyses and annotated significant SNPs (in exons and regulatory regions), demonstrating involvement of cardiac-related pathways and regulation of nearby genes.

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