Sensitive

Lung cancer or family history of lung cancer

near HCG22 · rs6457312

Where this position leads

Condition: Lung Cancer

rs6457312 Condition: Lung Cancer Lung Cancer Condition rs6457312 rs6457312 near HCG22

What the study found

Who was studied 29,266 European ancestry lung cancer cases, 48,843 European ancestry individuals with family history of lung cancer, 251,837 European ancestry controls.

The effect Each copy of the G allele carried 1.08 times the odds of Lung cancer or family history of lung cancer (95% confidence interval 1.058-1.099); p = 3 × 10−13.

How common The G allele had a frequency of about 40% in the people studied.

Where it sits Chromosome 6, band 6p21.33 — between genes, 8.1 kb from HCG22.

What each result means

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

Questions about rs6457312

What is rs6457312?

rs6457312 is a single position in the genome, in or near the near HCG22 gene. Published research associates it with lung cancer or family history of 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 rs6457312 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 rs6457312 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 rs6457312 come from?

GWAS Catalog, Journal of the National Cancer Institute 2022, PMID:35511172. 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 or family history of lung cancer (rs6457312). MyGeneLog™. https://www.mygenelog.com/variants/rs6457312

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