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GWAS Study

Gene-Based Variant Analysis of Whole-Exome Sequencing in Relation to Eosinophil Count.

Höglund J, Hadizadeh F, Ek WE et al.

35935937 PubMed ID
GWAS Study Type
365954 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

HJ
Höglund J
HF
Hadizadeh F
EW
Ek WE
KT
Karlsson T
Johansson Å
Chapter II

Abstract

Summary of the research findings

Eosinophils play important roles in the release of cytokine mediators in response to inflammation. Many associations between common genetic variants and eosinophils have already been reported, using single nucleotide polymorphism (SNP) array data. Here, we have analyzed 200,000 whole-exome sequences (WES) from the UK Biobank cohort and performed gene-based analyses of eosinophil count. We defined five different variant weighting schemes to incorporate information on both deleteriousness and frequency. A total of 220 genes in 55 distinct (>10 Mb apart) genomic regions were found to be associated with eosinophil count, of which seven genes (ALOX15, CSF2RB, IL17RA, IL33, JAK2, S1PR4, and SH2B3) are driven by rare variants, independent of common variants identified in genome-wide association studies. Two additional genes, NPAT and RMI1, have not been associated with eosinophil count before and are considered novel eosinophil loci. These results increase our knowledge about the effect of rare variants on eosinophil count, which can be of great value for further identification of therapeutic targets.

365,954 British ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

365954
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
U.K.
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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