The American Journal of Human GeneticsGeneticsPeer-reviewed journal article
An allelic series rare variant association test for candidate gene discovery
Zachary Ryan McCawiD, Colm T. O’DushlaineiD, Hari SomineniiD, Michael D. Bereket, Christoph KleiniD, Theofanis KaraletsosiD, Francesco Paolo CasaleiD, Daphne KolleriD, Thomas W. SoareiD
Abstract
Allelic series are of candidate therapeutic interest due to the existence of a dose-response relationship between the functionality of a gene and the degree or severity of a phenotype. We define an allelic series as a gene in which increasingly deleterious mutations lead to increasingly large phenotypic effects, and develop a gene-based rare variant association test specifically targeted for the identification of allelic series. Building on the well-known burden and sequence kernel association (SKAT) tests, we specify a variety of association models, covering different genetic architectures, and integrate these into a COding-variant Allelic Series Test (COAST). Through extensive simulations, we confirm that COAST maintains the type I error and improves power when the pattern of coding-variant effect sizes increases monotonically with mutational severity. We applied COAST to identify allelic series for 4 circulating lipid traits and 5 cell count traits among 145,735 subjects with available whole exome sequencing data from the UK Biobank. Compared with optimal SKAT (SKAT-O), COAST identified 29% more Bonferroni significant associations with circulating lipid traits, on average, and 82% more with cell count traits. All of the gene-trait associations identified by COAST have corroborating evidence either from rare-variant associations in the full cohort (Genebass, N = 400K), or from common variant associations in the GWAS catalog. In addition to detecting many gene-trait associations present in Genebass using only a fraction (36.9%) of the sample, COAST detects associations, such as ANGPTL4 with triglycerides, that are absent from Genebass but which have clear common variant support.
- organism: human
- assay: whole-exome sequencing
- research focus: GWAS / association mapping
- research focus: benchmarking
- research focus: variant effect prediction
- approach: statistical model
- Citations
- 26
- FWCI
- 4.48
- Field percentile
- top 4%
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