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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 408,112 British individuals.
The effect
Each copy of the G allele shifted the measure 0.0149 lower (95% confidence interval 0.011-0.019); p = 3 × 10−11.
How common The G allele had a frequency of about 45% in the people studied.
Where it sits Chromosome 14, band 14q32.32 — between genes, 15.2 kb from EIF5-DT.
What each result means
A/ANo copy of the version the research linked to Eosinophil count. This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to Eosinophil count. That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Eosinophil count. That is the strongest link of the three results. A link in a study is not a diagnosis.
rs10135205 is a single position in the genome, in or near the near EIF5-DT gene. Published research associates it with eosinophil count. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs10135205 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 rs10135205 come from?
GWAS Catalog, Cell 2020, PMID:32888494. 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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