Some genetic variants inherited from Neandertals may protect against developing severe COVID-19.
A new study looked at a stretch of DNA on chromosome 12 where a haplotype — a cluster of genetic variants that are inherited together — that affects susceptibility to the coronavirus is located. For each copy of the Neandertal haplotype a person inherited, the risk of needing intensive care fell approximately 22 percent, researchers report in the March 2 Proceedings of the National Academy of Sciences.
The variants may affect the activity or function of genes involved in a biochemical chain reaction that ends with the destruction of viral RNA, including the coronavirus’s. The protective variants are largely absent among people in sub-Saharan Africa, where few people carry genes inherited from Neandertals. About 25 to 30 percent of present-day people of Asian and European ancestry carry the protective variants. Some Black people in the Americas also inherited the protective haplotype, presumably from Asian, European or Native American ancestors.
Previously, researchers had found that a different haplotype on chromosome 3 that was inherited from Neandertals increases the risk of severe disease (SN:10/2/20). The results show that genetic inheritance can help or hinder the immune response to disease.

Science to restore speech is moving fast. Here’s what’s next
Toxic secrets are hiding in Arctic ice
Fossil fuel emissions are down in 2026. Green energy isn’t the reason
Drugs like Ozempic may help reverse chronic kidney disease
A high-fiber diet may clear away plastic in the gut
This may be the best evidence yet that dinosaur blood can fossilize
Climate crisis could push 141 million more women into extreme poverty
Sudan war: First suicide bombers, now long-range drone strikes are the norm
When deaths go uncounted: WHO flags dangerous blind spots in Africa’s health data
Security Council LIVE: South Sudan’s first elections loom amid rising violence