Deep learning identified genetic variants for COVID‐19‐related mortality among 28,097 affected cases in UK Biobank

Author:

Liu Zihuan1,Dai Wei1,Wang Shiying1,Yao Yisha1,Zhang Heping1ORCID

Affiliation:

1. Department of Biostatistics Yale University New Haven Connecticut USA

Abstract

AbstractAnalysis of host genetic components provides insights into the susceptibility and response to viral infection such as severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2), which causes coronavirus disease 2019 (COVID‐19). To reveal genetic determinants of susceptibility to COVID‐19 related mortality, we train a deep learning model to identify groups of genetic variants and their interactions that contribute to the COVID‐19 related mortality risk using the UK Biobank data (28,097 affected cases and 1656 deaths). We refer to such groups of variants as super variants. We identify 15 super variants with various levels of significance as susceptibility loci for COVID‐19 mortality. Specifically, we identify a super variant (odds ratio [OR] = 1.594, p = 5.47 × 10−9) on Chromosome 7 that consists of the minor allele of rs76398985, rs6943608, rs2052130, 7:150989011_CT_C, rs118033050, and rs12540488. We also discover a super variant (OR = 1.353, p = 2.87 × 10−8) on Chromosome 5 that contains rs12517344, rs72733036, rs190052994, rs34723029, rs72734818, 5:9305797_GTA_G, and rs180899355.

Funder

National Science Foundation

Publisher

Wiley

Subject

Genetics (clinical),Epidemiology

Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Peripheral Blood Omics and Other Multiplex-based Systems in Pulmonary and Critical Care Medicine;American Journal of Respiratory Cell and Molecular Biology;2023-10

2. Pros and cons of Mendelian randomization;Fertility and Sterility;2023-06

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