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. 2021 Jul 1;108(7):1350-1355.
doi: 10.1016/j.ajhg.2021.05.017. Epub 2021 Jun 3.

Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individuals

Jack A Kosmicki  1 Julie E Horowitz  1 Nilanjana Banerjee  1 Rouel Lanche  1 Anthony Marcketta  1 Evan Maxwell  1 Xiaodong Bai  1 Dylan Sun  1 Joshua D Backman  1 Deepika Sharma  1 Fabricio S P Kury  1 Hyun M Kang  1 Colm O'Dushlaine  1 Ashish Yadav  1 Adam J Mansfield  1 Alexander H Li  1 Kyoko Watanabe  1 Lauren Gurski  1 Shane E McCarthy  1 Adam E Locke  1 Shareef Khalid  1 Sean O'Keeffe  1 Joelle Mbatchou  1 Olympe Chazara  2 Yunfeng Huang  3 Erika Kvikstad  4 Amanda O'Neill  2 Paul Nioi  5 Meg M Parker  5 Slavé Petrovski  2 Heiko Runz  3 Joseph D Szustakowski  4 Quanli Wang  2 Emily Wong  6 Aldo Cordova-Palomera  6 Erin N Smith  6 Sandor Szalma  6 Xiuwen Zheng  7 Sahar Esmaeeli  7 Justin W Davis  7 Yi-Pin Lai  8 Xing Chen  8 Anne E Justice  9 Joseph B Leader  9 Tooraj Mirshahi  9 David J Carey  9 Anurag Verma  10 Giorgio Sirugo  10 Marylyn D Ritchie  10 Daniel J Rader  10 Gundula Povysil  11 David B Goldstein  12 Krzysztof Kiryluk  13 Erola Pairo-Castineira  14 Konrad Rawlik  15 Dorota Pasko  16 Susan Walker  16 Alison Meynert  17 Athanasios Kousathanas  16 Loukas Moutsianas  16 Albert Tenesa  18 Mark Caulfield  19 Richard Scott  20 James F Wilson  21 J Kenneth Baillie  22 Guillaume Butler-Laporte  23 Tomoko Nakanishi  24 Mark Lathrop  25 J Brent Richards  26 Regeneron Genetics CenterUKB Exome Sequencing ConsortiumMarcus Jones  1 Suganthi Balasubramanian  1 William Salerno  1 Alan R Shuldiner  1 Jonathan Marchini  1 John D Overton  1 Lukas Habegger  1 Michael N Cantor  1 Jeffrey G Reid  1 Aris Baras  1 Goncalo R Abecasis  27 Manuel A R Ferreira  28
Affiliations

Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individuals

Jack A Kosmicki et al. Am J Hum Genet. .

Abstract

Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) causes coronavirus disease 2019 (COVID-19), a respiratory illness that can result in hospitalization or death. We used exome sequence data to investigate associations between rare genetic variants and seven COVID-19 outcomes in 586,157 individuals, including 20,952 with COVID-19. After accounting for multiple testing, we did not identify any clear associations with rare variants either exome wide or when specifically focusing on (1) 13 interferon pathway genes in which rare deleterious variants have been reported in individuals with severe COVID-19, (2) 281 genes located in susceptibility loci identified by the COVID-19 Host Genetics Initiative, or (3) 32 additional genes of immunologic relevance and/or therapeutic potential. Our analyses indicate there are no significant associations with rare protein-coding variants with detectable effect sizes at our current sample sizes. Analyses will be updated as additional data become available, and results are publicly available through the Regeneron Genetics Center COVID-19 Results Browser.

Keywords: COVID-19; SARS-CoV-2; TLR7; ZC3HAV1; association; burden; exome sequencing; genetics; rare variants.

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