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Allergen component sensitization (Hevea brasiliensis 8)

near HLA-DRB1 · rs2760979

Strength of the evidence

1 / 4

Its strongest genetic-study result is p = 10−7, with 1 associations in the GWAS Catalog.

How this is scored

4: ClinVar disease-causing, reviewed by an expert panel or a guideline (3–4 stars). 3: ClinVar, several labs agreeing (2 stars), or a genetic study at p ≤ 10−50. 2: ClinVar from one lab (1 star), or p ≤ 10−20. 1: ClinVar submitted without criteria (0 stars), or genome-wide significance (p ≤ 5×10−8). The higher of the two counts. It says how solid the evidence is, not whether it matters for a particular person.

What the study found

Who was studied 50 Japanese ancestry pediatric cases, 514 Japanese ancestry pediatric controls.

The effect Each copy of the T allele carried 5.20 times the odds of Allergen component sensitization (Hevea brasiliensis 8) (95% confidence interval 2.933-9.206); p = 4 × 10−8.

How common The T allele had a frequency of about 13% in the people studied.

Where it sits Chromosome 6, band 6p21.32 — between genes, 7.2 kb from HLA-DRB1.

What each result means

A/A No copy of the version the research linked to Allergen component sensitization (Hevea brasiliensis 8). This is the starting point the study compared everyone against.
A/T One copy of the version the research linked to Allergen component sensitization (Hevea brasiliensis 8). That is a smaller link than two copies.
T/T Two 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.
Source

Questions about rs2760979

What is rs2760979?

rs2760979 is a single position in the genome, in or near the near 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 rs2760979 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 rs2760979 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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Allergen component sensitization (Hevea brasiliensis 8) (rs2760979). MyGeneLog™. https://www.mygenelog.com/variants/rs2760979

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