As the coronavirus emerged, so did a mystery: Why did some who got infected never develop symptoms?
One likely explanation is it may be a person's lucky genes.
A new study published Wednesday in the scientific journal Nature suggests people with a specific version of a gene were far more likely to experience an asymptomatic infection than those without.
The relevant set of genes is known as the human leukocyte antigen, or HLA.
"This is the first time where, in a really rigorous and robust way, anybody has shown that there is a clear, definitive genetic underpinning to asymptomatic disease [from the coronavirus] — not all asymptomatic disease, but some subset of people who stay asymptomatic," said UC San Francisco neurology professor Jill Hollenbach, a co-author of the study.
Hollenbach and other researchers recruited some 30,000 people for the study — all of whom already had genetic data on file because they had registered as potential bone marrow donors with the National Marrow Donor Program.
Scientists asked those individuals to join the COVID-19 Citizen Science study, organized by researchers at UC San Francisco, and to use a smartphone app to track their coronavirus test results and any symptoms.
Researchers had a significant sample size of coronavirus-positive patients with European ancestry to generate meaningful data; there were too few test-positive participants of other ancestries for those results to be significant.