Eosinophil cationic protein levels and Eosinophil-derived neurotoxin levels
ARHGAP25 · rs116571378
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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 1,018 European ancestry individuals; replicated in 153 French-Canadian founder ancestry individuals.
The effect
The reported allele is T; the catalogue records no effect size
; p = 4 × 10−10.
How common The T allele had a frequency of about 4% in the people studied.
Where it sits Chromosome 2, band 2p13.3 — in an intron of ARHGAP25.
What each result means
C/CNo copy of the version the research linked to Eosinophil cationic protein levels and Eosinophil-derived neurotoxin levels. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Eosinophil cationic protein levels and Eosinophil-derived neurotoxin levels. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Eosinophil cationic protein levels and Eosinophil-derived neurotoxin levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
The Journal of allergy and clinical immunology · 2022 · PMID 35671886
Questions about rs116571378
What is rs116571378?
rs116571378 is a single position in the genome, in or near the ARHGAP25 gene. Published research associates it with eosinophil cationic protein levels and eosinophil-derived neurotoxin levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs116571378 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 rs116571378 come from?
GWAS Catalog, The Journal of allergy and clinical immunology 2022, PMID:35671886. 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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Eosinophil cationic protein levels and Eosinophil-derived neurotoxin levels (rs116571378). MyGeneLog™. https://www.mygenelog.com/variants/rs116571378