Abstract
To date, the locus with the most robust human genetic association to COVID-19 severity is 3p21.31. Here, we integrate genome-scale CRISPR loss-of-function screens and eQTLs in diverse cell types and tissues to pinpoint genes underlying COVID-19 risk. Our findings identify SLC6A20 and CXCR6 as putative causal genes that modulate COVID-19 risk and highlight the usefulness of this integrative approach to bridge the divide between correlational and causal studies of human biology.
Original language | English |
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Article number | 242 |
Journal | Genome Biology |
Volume | 22 |
Issue number | 1 |
DOIs | |
State | Published - Dec 2021 |
Keywords
- COVID-19
- CRISPR
- GWAS
- SARS-CoV-2
- eQTL