@article{Baillie_J-2022_101362,
title = {Exome-wide association study to identify rare variants influencing COVID-19 outcomes:Results from the Host Genetics Initiative},
author = {Baillie, J.},
month = {nov},
year = {2022},
abstract = {Host genetics is a key determinant of COVID-19 outcomes. Previously, the COVID-19 Host Genetics Initiative genome-wide association study used common variants to identify multiple loci associated with COVID-19 outcomes. However, variants with the largest impact on COVID-19 outcomes are expected to be rare in the population. Hence, studying rare variants may provide additional insights into disease susceptibility and pathogenesis, thereby informing therapeutics development. Here, we combined whole-exome and whole-genome sequencing from 21 cohorts across 12 countries and performed rare variant exome-wide burden analyses for COVID-19 outcomes. In an analysis of 5,085 severe disease cases and 571,737 controls, we observed that carrying a rare deleterious variant in the SARS-CoV-2 sensor toll-like receptor TLR7 (on chromosome X) was associated with a 5.3-fold increase in severe disease (95% CI: 2.75-10.05, p = 5.41x10-7). This association was consistent across sexes. These results further support TLR7 as a genetic determinant of severe disease and suggest that larger studies on rare variants influencing COVID-19 outcomes could provide additional insights.},
pages = {1-26},
volume = {18},
issue = {11},
journal = {PLoS Genetics},
publisher = {Public Library of Science},
url = {https://doi.org/10.1371/journal.pgen.1010367},
}
