Sensitive

Chronic obstructive pulmonary disease liability (machine learning-based score)

near ME3 · rs11607392

What the study found

Who was studied 325,027 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.028 lower (95% confidence interval 0.022-0.034); p = 5 × 10−20.

Where it sits Chromosome 11, band 11q14.2 — between genes, 53.7 kb from ME3.

What each result means

C/C No copy of the version the research linked to Chronic obstructive pulmonary disease liability (machine learning-based score). This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to Chronic obstructive pulmonary disease liability (machine learning-based score). That is a smaller link than two copies.
T/T Two copies of the version the research linked to Chronic obstructive pulmonary disease liability (machine learning-based score). That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs11607392

What is rs11607392?

rs11607392 is a single position in the genome, in or near the near ME3 gene. Published research associates it with chronic obstructive pulmonary disease liability (machine learning-based score). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs11607392 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 rs11607392 come from?

GWAS Catalog, Nature genetics 2023, PMID:37069358. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

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Chronic obstructive pulmonary disease liability (machine learning-based score) (rs11607392). MyGeneLog™. https://www.mygenelog.com/variants/rs11607392

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