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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 66 Japanese ancestry pediatric cases, 498 Japanese ancestry pediatric controls.
The effect
Each copy of the G allele carried 4.03 times the odds of Allergen component sensitization (Ambrosia artemisiifolia 1) (95% confidence interval 2.483-6.527); p = 2 × 10−8.
How common The G allele had a frequency of about 11% in the people studied.
Where it sits Chromosome 14, band 14q32.33 — between genes, 3.1 kb from IGHVII-62-1.
What each result means
C/CNo copy of the version the research linked to Allergen component sensitization (Ambrosia artemisiifolia 1). This is the starting point the study compared everyone against.
C/GOne copy of the version the research linked to Allergen component sensitization (Ambrosia artemisiifolia 1). That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Allergen component sensitization (Ambrosia artemisiifolia 1). 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. Global · 2023 · PMID 37780799 · open access
Questions about rs10129888
What is rs10129888?
rs10129888 is a single position in the genome, in or near the near IGHVII-62-1 gene. Published research associates it with allergen component sensitization (ambrosia artemisiifolia 1). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs10129888 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 rs10129888 come from?
GWAS Catalog, The journal of allergy and clinical immunology. Global 2023, PMID:37780799. 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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