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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 1,240 African ancestry cases, 22,582 African ancestry controls, 2,480 Hispanic or Latin American cases, 34,308 Hispanic or Latin American controls, 36,474 European ancestry cases, 1,339,760 European ancestry controls, 162 South Asian ancestry cases, 10,914 South Asian ancestry controls.
The effect
Each copy of the A allele carried 0.92 times the odds of Influenza (95% confidence interval 0.906-0.934); p = 4 × 10−28.
How common The A allele had a frequency of about 47% in the people studied.
Where it sits Chromosome 21, band 21q22.2 — in the 3′ untranslated region of B3GALT5.
What each result means
A/ATwo copies of the version the research linked to Influenza. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/GOne copy of the version the research linked to Influenza. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Influenza. This is the starting point the study compared everyone against.
Nature genetics · 2024 · PMID 39103650 · open access
Questions about rs2837112
What is rs2837112?
rs2837112 is a single position in the genome, in or near the B3GALT5 gene. Published research associates it with influenza. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs2837112 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 rs2837112 come from?
GWAS Catalog, Nature genetics 2024, PMID:39103650. 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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