Frontiers in Genetics (Feb 2022)

Genetic Loci Associated With COVID-19 Positivity and Hospitalization in White, Black, and Hispanic Veterans of the VA Million Veteran Program

  • Gina M. Peloso,
  • Gina M. Peloso,
  • Catherine Tcheandjieu,
  • Catherine Tcheandjieu,
  • Catherine Tcheandjieu,
  • John E. McGeary,
  • John E. McGeary,
  • Daniel C. Posner,
  • Yuk-Lam Ho,
  • Jin J. Zhou,
  • Jin J. Zhou,
  • Austin T. Hilliard,
  • Jacob Joseph,
  • Jacob Joseph,
  • Jacob Joseph,
  • Christopher J. O’Donnell,
  • Christopher J. O’Donnell,
  • Christopher J. O’Donnell,
  • Jimmy T. Efird,
  • Dana C. Crawford,
  • Dana C. Crawford,
  • Dana C. Crawford,
  • Dana C. Crawford,
  • Wen-Chih Wu,
  • Wen-Chih Wu,
  • Mehrdad Arjomandi,
  • Mehrdad Arjomandi,
  • VA Million Veteran Program COVID-19 Science Initiative,
  • Yan V. Sun,
  • Yan V. Sun,
  • Themistocles L Assimes,
  • Themistocles L Assimes,
  • Themistocles L Assimes,
  • Jennifer E. Huffman

DOI
https://doi.org/10.3389/fgene.2021.777076
Journal volume & issue
Vol. 12

Abstract

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SARS-CoV-2 has caused symptomatic COVID-19 and widespread death across the globe. We sought to determine genetic variants contributing to COVID-19 susceptibility and hospitalization in a large biobank linked to a national United States health system. We identified 19,168 (3.7%) lab-confirmed COVID-19 cases among Million Veteran Program participants between March 1, 2020, and February 2, 2021, including 11,778 Whites, 4,893 Blacks, and 2,497 Hispanics. A multi-population genome-wide association study (GWAS) for COVID-19 outcomes identified four independent genetic variants (rs8176719, rs73062389, rs60870724, and rs73910904) contributing to COVID-19 positivity, including one novel locus found exclusively among Hispanics. We replicated eight of nine previously reported genetic associations at an alpha of 0.05 in at least one population-specific or the multi-population meta-analysis for one of the four MVP COVID-19 outcomes. We used rs8176719 and three additional variants to accurately infer ABO blood types. We found that A, AB, and B blood types were associated with testing positive for COVID-19 compared with O blood type with the highest risk for the A blood group. We did not observe any genome-wide significant associations for COVID-19 severity outcomes among those testing positive. Our study replicates prior GWAS findings associated with testing positive for COVID-19 among mostly White samples and extends findings at three loci to Black and Hispanic individuals. We also report a new locus among Hispanics requiring further investigation. These findings may aid in the identification of novel therapeutic agents to decrease the morbidity and mortality of COVID-19 across all major ancestral populations.

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