Nature GeneticsGenetic & Genomic MedicinePeer-reviewed journal article
The UGT2A1/UGT2A2 locus is associated with COVID-19-related anosmia
Janie F. Shelton, Anjali J. Shastri, Kipper Fletez‐BrantiD, The 23andMe COVID-19 Team, Adam AutoniD, Adrian Chubb, Alison Fitch, Alison Kung, Amanda Altman, Andy Kill, Antony SymonsiD, Catherine H. Weldon, Daniella CokeriD, Jason Tan, Jeff Pollard, Jey C. McCreight, Jessica BielenbergiD, J. B. MatthewsiD, Johnny W. LeeiD, Lindsey Tran, Maya Lowe, Monica Royce, Nate Tang, Pooja GandhiiD, Raffaello d’Amore, , Yiwen Zheng
Abstract
Loss of sense of smell is a characteristic symptom of infection with SARS-CoV-2. However, specific mechanisms linking infection with loss of smell are poorly understood. Using self-reported symptom data from the 23andMe COVID-19 study, we describe the demographic patterns associated with COVID-19 related anosmia, and find the symptom is more often reported in women and younger respondents, and less often by those of East Asian and African American ancestry compared to those of European ancestry. We ran a trans-ethnic genome-wide association study (GWAS) comparing loss of smell or taste (n=47,298) with no loss of smell or taste (n=22,543) among those with a positive SARS-CoV-2 test result. We identified an association (rs7688383) in the vicinity of the UGT2A1 and UGT2A2 genes (OR=1.115, p-value=4x10-15), which have been linked to olfactory function. These results may shed light on the biological mechanisms underlying COVID-19 related anosmia.
- organism: human
- assay: GWAS summary statistics
- research focus: GWAS / association mapping
- approach: statistical model
- Citations
- 124
- FWCI
- 17.33
- Field percentile
- top 1%
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