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Glioma

CCDC26 · rs891835

Where this position leads

Condition: Glioma

rs891835 Condition: Glioma Glioma Condition rs891835 rs891835 CCDC26

What the study found

Who was studied 1,878 European ancestry cases, 3,670 European ancestry controls; replicated in 2,545 European ancestry cases, 2,953 European ancestry controls.

The effect Each copy of the G allele carried 1.24 times the odds of Glioma (95% confidence interval 1.17-1.30); p = 8 × 10−11.

How common The G allele had a frequency of about 79% in the people studied.

Where it sits Chromosome 8, band 8q24.21 — in an intron of CCDC26.

What each result means

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

Questions about rs891835

What is rs891835?

rs891835 is a single position in the genome, in or near the CCDC26 gene. Published research associates it with glioma. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs891835 linked to?

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

Does having rs891835 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 rs891835 come from?

GWAS Catalog, Nat Genet 2009, PMID:19578367. 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.

Glioma (rs891835). MyGeneLog™. https://www.mygenelog.com/variants/rs891835

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