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Stands on its own.
Nothing else here links to this position yet — but the page above is the point: what the
research found, what each genotype means, and where it came from, in language you can
read. Links to conditions, drugs and the senses appear automatically if we write them.
What the study found
Who was studied 763 African ancestry cases, 24,850 African ancestry controls, 218 admixed American ancestry cases, 94,318 admixed American ancestry controls, 414 East Asian ancestry cases, 816 East Asian ancestry controls, 16,627 European ancestry cases, 749,207 European ancestry controls, 3,533 European, African or admixed American ancestry cases, 1,700 European, African or admixed American ancestry controls, 1,171 South Asian ancestry cases, 5,489 South Asian ancestry controls, 93 other admixed ancestry cases, 645 other admixed ancestry controls, 22,637 cases, 2,052,436 controls.
The effect
Each copy of the A allele carried 0.72 times the odds of COVID-19 (hospitalized covid vs population) (95% confidence interval 0.7-0.74); p = 4 × 10−103.
Where it sits Chromosome 3, band 3p21.31 — between genes, 7.7 kb from SLC6A20.
What each result means
A/ATwo copies of the version the research linked to COVID-19 (hospitalized covid vs population). That is the strongest link of the three results. A link in a study is not a diagnosis.
A/COne copy of the version the research linked to COVID-19 (hospitalized covid vs population). That is a smaller link than two copies.
C/CNo copy of the version the research linked to COVID-19 (hospitalized covid vs population). This is the starting point the study compared everyone against.
rs17078346 is a single position in the genome, in or near the near SLC6A20 gene. Published research associates it with covid-19 (hospitalized covid vs population). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs17078346 mean I will get this?
No. Common variants like this one move a probability slightly and, on their own, rarely decide anything about one person. Nothing on this page is a diagnosis, and health decisions should be made with a clinician who can see your whole picture.
Where does the information about rs17078346 come from?
GWAS Catalog, Nature 2023, PMID:37198478. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
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Quoting this page
Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.
COVID-19 (hospitalized covid vs population) (rs17078346). MyGeneLog™. https://www.mygenelog.com/variants/rs17078346