Deletion of the NKG2C receptor encoding KLRC2 gene and HLA-E variants are risk factors for severe COVID-19.
Hannes VietzenAlexander ZoufalyMarianna TraugottJudith AberleStephan W AberleElisabeth Puchhammer-StöcklPublished in: Genetics in medicine : official journal of the American College of Medical Genetics (2021)
Our data show that these genetic variants in the NKG2C/HLA-E axis have a significant impact on the development of severe SARS-CoV-2 infections, and may help to identify patients at high-risk for severe COVID-19.