Sensitive

Lung cancer

near ACTRT3 · rs187047327

Where this position leads

Condition: Lung Cancer

rs187047327 Condition: Lung Cancer Lung Cancer Condition rs187047327 rs187047327 near ACTRT3

What the study found

Who was studied 59,774 European ancestry cases, 1,416,415 European ancestry controls, 11,773 East Asian ancestry cases, 288,419 East Asian ancestry controls, 4,782 African ancestry cases, 122,496 African ancestry controls, 624 Hispanic/Latino American ancestry cases, 59,042 Hispanic/Latino American ancestry controls.

The effect Each copy of the A allele shifted the measure 0.0531 higher (95% confidence interval 0.036-0.07); p = 2 × 10−9.

How common The A allele had a frequency of about 71% in the people studied.

Where it sits Chromosome 3, band 3q26.2 — between genes, 1.3 kb from ACTRT3.

What each result means

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

Questions about rs187047327

What is rs187047327?

rs187047327 is a single position in the genome, in or near the near ACTRT3 gene. Published research associates it with lung cancer. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs187047327 linked to?

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

Does having rs187047327 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 rs187047327 come from?

GWAS Catalog, Nature communications 2026, PMID:42364979. 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.

Lung cancer (rs187047327). MyGeneLog™. https://www.mygenelog.com/variants/rs187047327

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