Sensitive

Interstitial lung disease

ATP11A · rs1278769

Where this position leads

Condition: Interstitial Lung Disease

rs1278769 Condition: Interstitial Lung Disease Interstitial Lung Disease Condition rs1278769 rs1278769 ATP11A

What the study found

Who was studied 1,161 European ancestry cases, 4,683 European ancestry controls; replicated in 876 European ancestry cases, 1,890 European ancestry controls.

The effect Each copy of the G allele carried 1.27 times the odds of Interstitial lung disease (95% confidence interval 1.14-1.39); p = 7 × 10−9.

How common The G allele had a frequency of about 76% in the people studied.

Where it sits Chromosome 13, band 13q34 — in the 3′ untranslated region of ATP11A.

What each result means

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

Questions about rs1278769

What is rs1278769?

rs1278769 is a single position in the genome, in or near the ATP11A gene. Published research associates it with interstitial lung 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 rs1278769 linked to?

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

Does having rs1278769 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 rs1278769 come from?

GWAS Catalog, Nat Genet 2013, PMID:23583980. 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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Interstitial lung disease (rs1278769). MyGeneLog™. https://www.mygenelog.com/variants/rs1278769

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