Sensitive

Colorectal cancer

LAMC1 · rs10911251

Where this position leads

Condition: Colorectal Cancer

rs10911251 Condition: Colorectal Cancer Colorectal Cancer Condition rs10911251 rs10911251 LAMC1

What each result means

A/A Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Colorectal cancer compared to the general population. (GWAS Catalog, J Natl Cancer Inst 2018, PMID:29917119)
A/C Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Colorectal cancer. (GWAS Catalog, J Natl Cancer Inst 2018, PMID:29917119)
C/C Published research associates this genotype with typical/baseline likelihood of Colorectal cancer — no copies of the reported risk allele. (GWAS Catalog, J Natl Cancer Inst 2018, PMID:29917119)

Source: GWAS Catalog, J Natl Cancer Inst 2018, PMID:29917119

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 rs10911251

What is rs10911251?

rs10911251 is a single position in the genome, in or near the LAMC1 gene. Published research associates it with colorectal 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 rs10911251 linked to?

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

What do people read about alongside rs10911251?

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 rs10911251 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 rs10911251 come from?

GWAS Catalog, J Natl Cancer Inst 2018, PMID:29917119. 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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