Eosinophil cationic protein levels and Eosinophil-derived neurotoxin levels
near RN7SL189P · rs67049014
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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 A; the catalogue records no effect size
; p = 1 × 10−13.
How common The A allele had a frequency of about 26% in the people studied.
Where it sits Chromosome 14, band 14q11.2 — between genes, 0.6 kb from RN7SL189P.
What each result means
A/ATwo 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.
A/GOne 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.
G/GNo 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.
The Journal of allergy and clinical immunology · 2022 · PMID 35671886
Questions about rs67049014
What is rs67049014?
rs67049014 is a single position in the genome, in or near the near RN7SL189P 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 rs67049014 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 rs67049014 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 (rs67049014). MyGeneLog™. https://www.mygenelog.com/variants/rs67049014