Sensitive

Chronic obstructive pulmonary disease

RPL23 · rs34727469

Where this position leads

Condition: Chronic Obstructive Pulmonary Disease (COPD)

rs34727469 Condition: Chronic Obstructive Pulmonary Disease (COPD) Chronic Obstructive Pulmonary Disea… Condition rs34727469 rs34727469 RPL23

What the study found

Who was studied 35,735 cases, 222,076 controls.

The effect Each copy of the T allele carried 1.09 times the odds of Chronic obstructive pulmonary disease (95% confidence interval 1.06-1.12); p = 1 × 10−8.

How common The T allele had a frequency of about 14% in the people studied.

Where it sits Chromosome 17, band 17q12 — between genes, 3.9 kb from EPOP.

What each result means

C/C No copy of the version the research linked to Chronic obstructive pulmonary disease. 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. That is a smaller link than two copies.
T/T Two copies of the version the research linked to Chronic obstructive pulmonary disease. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs34727469

What is rs34727469?

rs34727469 is a single position in the genome, in or near the RPL23 gene. Published research associates it with chronic obstructive pulmonary disease. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs34727469 linked to?

On MyGeneLog this position is linked to Chronic Obstructive Pulmonary Disease (COPD). The research behind each link, and its sources, are set out on that condition page.

Does having rs34727469 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 rs34727469 come from?

GWAS Catalog, Nature genetics 2019, PMID:30804561. 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 (rs34727469). MyGeneLog™. https://www.mygenelog.com/variants/rs34727469

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