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Alternative splicing of OAS1 alters the risk for severe COVID-19.

Jennifer E HuffmanGuillaume Butler-LaporteAtlas KhanTheodore G DrivasGina M PelosoTomoko NakanishiAnurag VermaKrzysztof KirylukJohn Brent RichardsHugo Zeberg
Published in: medRxiv : the preprint server for health sciences (2021)
A locus containing OAS1/2/3 has been identified as a risk locus for severe COVID-19 among Europeans ancestry individuals, with a protective haplotype of ∼75 kilobases derived from Neanderthals. Here, we show that among several potentially causal variants at this locus, a splice variant of OAS1 occurs in people of African ancestry independently of the Neanderthal haplotype and confers protection against COVID-19 of a magnitude similar to that seen in individuals without African ancestry.
Keyphrases
  • coronavirus disease
  • genome wide association study
  • sars cov
  • early onset
  • respiratory syndrome coronavirus
  • copy number
  • gene expression
  • dna methylation
  • drug induced