Standard
Eosinophil count
IL18R1 · rs10208293
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 A allele shifted the measure 0.0705 lower (95% confidence interval 0.065-0.076); p = 3 × 10−152.
How common The A allele had a frequency of about 29% in the people studied.
Where it sits Chromosome 2, band 2q12.1 — in an intron of IL1RL1.
What each result means
A/A
Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Eosinophil count compared to the general population.
A/G
Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Eosinophil count.
G/G
Published research associates this genotype with typical/baseline likelihood of Eosinophil count — no copies of the reported risk allele.
Source
The Polygenic and Monogenic Basis of Blood Traits and Diseases
Vuckovic D,
Bao EL,
Akbari P,
Lareau CA,
Mousas A,
Jiang T,
Chen MH,
Raffield LM,
Tardaguila M,
Huffman JE,
Ritchie SC,
Megy K
and 100 more — show all
Ponstingl H,
Penkett CJ,
Albers PK,
Wigdor EM,
Sakaue S,
Moscati A,
Manansala R,
Lo KS,
Qian H,
Akiyama M,
Bartz TM,
Ben-Shlomo Y,
Beswick A,
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Bottinger EP,
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van Rooij FJA,
Chitrala KN,
Wilson PWF,
Choquet H,
Danesh J,
Di Angelantonio E,
Dimou N,
Ding J,
Elliott P,
Esko T,
Evans MK,
Felix SB,
Floyd JS,
Broer L,
Grarup N,
Guo MH,
Guo Q,
Greinacher A,
Haessler J,
Hansen T,
Howson JMM,
Huang W,
Jorgenson E,
Kacprowski T,
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Kanai M,
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Lange LA,
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Liu Y,
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Manichaikul A,
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Mononen N,
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Preuss M,
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Raitakari OT,
Rich SS,
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Rosen JD,
Rotter JI,
Schubert P,
Spracklen CN,
Surendran P,
Tang H,
Tardif JC,
Ghanbari M,
Völker U,
Völzke H,
Watkins NA,
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Cai N,
Kundu K,
Watt SB,
Walter K,
Zonderman AB,
Cho K,
Li Y,
Loos RJF,
Knight JC,
Georges M,
Stegle O,
Evangelou E,
Okada Y,
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Cell · 2020 · PMID 32888494 · open access
Questions about rs10208293
What is rs10208293?
rs10208293 is a single position in the genome, in or near the IL18R1 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 rs10208293 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 rs10208293 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.
Quoting this page
Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.
Eosinophil count (rs10208293). MyGeneLog™. https://www.mygenelog.com/variants/rs10208293
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