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Asthma

LINC01807 · rs3732192

Where this position leads

Condition: Asthma

rs3732192 Condition: Asthma Asthma Condition rs3732192 rs3732192 LINC01807

What the study found

Who was studied 38,369 European ancestry cases, 411,131 European ancestry controls, 13,015 East Asian ancestry cases, 162,933 East Asian ancestry controls.

The effect Each copy of the C allele shifted the measure 0.073 lower (95% confidence interval 0.048-0.098); p = 6 × 10−9.

Where it sits Chromosome 2, band 2q36.3 — in an intron of LINC01807.

What each result means

C/C Two copies of the version the research linked to Asthma. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/T One copy of the version the research linked to Asthma. That is a smaller link than two copies.
T/T No copy of the version the research linked to Asthma. This is the starting point the study compared everyone against.
Source

Questions about rs3732192

What is rs3732192?

rs3732192 is a single position in the genome, in or near the LINC01807 gene. Published research associates it with asthma. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs3732192 linked to?

On MyGeneLog this position is linked to Asthma. The research behind each link, and its sources, are set out on that condition page.

Does having rs3732192 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 rs3732192 come from?

GWAS Catalog, Nature genetics 2021, PMID:34594039. 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.

Asthma (rs3732192). MyGeneLog™. https://www.mygenelog.com/variants/rs3732192

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