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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 50 Japanese ancestry pediatric cases, 514 Japanese ancestry pediatric controls.
The effect
Each copy of the A allele carried 9.26 times the odds of Allergen component sensitization (Hevea brasiliensis 8) (95% confidence interval 4.648-18.453); p = 5 × 10−10.
How common The A allele had a frequency of about 10% in the people studied.
Where it sits Chromosome 6, band 6p21.32 — in an intron of HLA-DRB1.
What each result means
A/ATwo copies of the version the research linked to Allergen component sensitization (Hevea brasiliensis 8). That is the strongest link of the three results. A link in a study is not a diagnosis.
A/TOne copy of the version the research linked to Allergen component sensitization (Hevea brasiliensis 8). That is a smaller link than two copies.
T/TNo copy of the version the research linked to Allergen component sensitization (Hevea brasiliensis 8). This is the starting point the study compared everyone against.
The journal of allergy and clinical immunology. Global · 2023 · PMID 37780799 · open access
Questions about rs1289784088
What is rs1289784088?
rs1289784088 is a single position in the genome, in or near the HLA-DRB1 gene. Published research associates it with allergen component sensitization (hevea brasiliensis 8). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs1289784088 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 rs1289784088 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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