Sensitive

Lung adenocarcinoma

CLPTM1L · rs31489

Stands on its own. Nothing else here links to this position yet — but the page above is the point: what the research found, what each genotype means, and where it came from, in language you can read. Links to conditions, drugs and the senses appear automatically if we write them.

What each result means

A/A Published research associates this genotype with typical/baseline likelihood of Lung adenocarcinoma — no copies of the reported risk allele. (GWAS Catalog, Am J Hum Genet 2009, PMID:19836008)

A/C Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Lung adenocarcinoma. (GWAS Catalog, Am J Hum Genet 2009, PMID:19836008)

C/C Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Lung adenocarcinoma compared to the general population. (GWAS Catalog, Am J Hum Genet 2009, PMID:19836008)

Source: GWAS Catalog, Am J Hum Genet 2009, PMID:19836008

Questions about rs31489

What is rs31489?

rs31489 is a single position in the genome, in or near the CLPTM1L gene. Published research associates it with lung adenocarcinoma. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs31489 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 rs31489 come from?

GWAS Catalog, Am J Hum Genet 2009, PMID:19836008. 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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