Sensitive

Colorectal cancer

near LINC01271 · rs11699816

Where this position leads

Condition: Colorectal Cancer

rs11699816 Condition: Colorectal Cancer Colorectal Cancer Condition rs11699816 rs11699816 near LINC012…

What the study found

Who was studied 15,714 European ancestry cases, 621,182 European ancestry controls, 7,062 East Asian ancestry cases, 195,745 East Asian ancestry controls.

The effect Each copy of the T allele shifted the measure 0.0553 lower; p = 2 × 10−11.

Where it sits Chromosome 20, band 20q13.13 — between genes, 40.6 kb from LINC01271.

What each result means

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

Questions about rs11699816

What is rs11699816?

rs11699816 is a single position in the genome, in or near the near LINC01271 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 rs11699816 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.

Does having rs11699816 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 rs11699816 come from?

GWAS Catalog, Genome medicine 2024, PMID:38872215. 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.

Colorectal cancer (rs11699816). MyGeneLog™. https://www.mygenelog.com/variants/rs11699816

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