Sensitive

Lung cancer

TP63 · rs4488809

Where this position leads

Condition: Lung Cancer

rs4488809 Condition: Lung Cancer Lung Cancer Condition rs4488809 rs4488809 TP63

What each result means

C/C Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Lung cancer compared to the general population. (GWAS Catalog, Nat Genet 2012, PMID:23143601)
C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Lung cancer. (GWAS Catalog, Nat Genet 2012, PMID:23143601)
T/T Published research associates this genotype with typical/baseline likelihood of Lung cancer — no copies of the reported risk allele. (GWAS Catalog, Nat Genet 2012, PMID:23143601)

Source: GWAS Catalog, Nat Genet 2012, PMID:23143601

What people read about alongside this

Papers in Europe PMC whose title or abstract names both this rsID and that subject. A shared paper means somebody wrote about the two together — it is not a claim that this position explains the subject.

Questions about rs4488809

What is rs4488809?

rs4488809 is a single position in the genome, in or near the TP63 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 rs4488809 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.

What do people read about alongside rs4488809?

Subjects that appear in the title or abstract of the same papers as this rsID include infection and immunity (1 papers). A shared paper means somebody wrote about the two together; it is not a claim that this position explains the topic.

Does having rs4488809 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 rs4488809 come from?

GWAS Catalog, Nat Genet 2012, PMID:23143601. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

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