Sensitive

Colorectal cancer

ANKRD19P · rs757853362

Where this position leads

Condition: Colorectal Cancer

rs757853362 Condition: Colorectal Cancer Colorectal Cancer Condition rs757853362 rs757853362 ANKRD19P

What the study found

Who was studied 4,988 European ancestry cases, 310,272 European ancestry controls.

The effect Each copy of the T allele shifted the measure 2.05 higher (95% confidence interval 1.36-2.73); p = 5 × 10−9.

Where it sits Chromosome 9, band 9q22.31 — in an intron of ANKRD19P.

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 rs757853362

What is rs757853362?

rs757853362 is a single position in the genome, in or near the ANKRD19P 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 rs757853362 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 rs757853362 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 rs757853362 come from?

GWAS Catalog, Scientific reports 2024, PMID:38538606. 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 (rs757853362). MyGeneLog™. https://www.mygenelog.com/variants/rs757853362

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