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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 98,055 African American or Afro-Caribbean individuals, 47,410 Hispanic or Latin American individuals, 4,652 East Asian ancestry individuals, 335,542 European ancestry individuals.
The effect
Each copy of the C allele shifted the measure 0.0241 lower (95% confidence interval 0.017-0.031); p = 1 × 10−12.
How common The C allele had a frequency of about 71% in the people studied.
Where it sits Chromosome 13, band 13q14.11 — between genes, 1.4 kb from LINC02341.
What each result means
C/CPublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of eosinophil (fraction, mean, inv-norm transformed) compared to the general population.
C/TPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with eosinophil (fraction, mean, inv-norm transformed).
T/TPublished research associates this genotype with typical/baseline likelihood of eosinophil (fraction, mean, inv-norm transformed) — no copies of the reported risk allele.
Science (New York, N.Y.) · 2024 · PMID 39024449 · open access
Questions about rs2324919
What is rs2324919?
rs2324919 is a single position in the genome, in or near the near LINC02341 gene. Published research associates it with eosinophil (fraction, mean, inv-norm transformed). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs2324919 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 rs2324919 come from?
GWAS Catalog, Science (New York, N.Y.) 2024, PMID:39024449. 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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