Sensitive

Osteoarthritis

DAGLB · rs113907280

Where this position leads

Condition: Knee Osteoarthritis

rs113907280 Condition: Knee Osteoarthritis Knee Osteoarthritis Condition rs113907280 rs113907280 DAGLB

What the study found

Who was studied 140,025 European ancestry cases, 344,349 European ancestry controls, 140,025 South Asian ancestry cases, 344,349 South Asian ancestry controls, 140,025 East Asian ancestry cases, 344,349 East Asian ancestry controls, 140,025 African ancestry cases, 344,349 African ancestry controls, 140,025 Hispanic or Latin American cases, 344,349 Hispanic or Latin American controls.

The effect Each copy of the T allele carried 0.99 times the odds of Osteoarthritis (95% confidence interval 0.99-0.99); p = 2 × 10−10.

How common The T allele had a frequency of about 80% in the people studied.

Where it sits Chromosome 7, band 7p22.1 — in an intron of DAGLB.

What each result means

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

Questions about rs113907280

What is rs113907280?

rs113907280 is a single position in the genome, in or near the DAGLB gene. Published research associates it with osteoarthritis. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs113907280 linked to?

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

Does having rs113907280 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 rs113907280 come from?

GWAS Catalog, Nature genetics 2022, PMID:36411363. 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.

Osteoarthritis (rs113907280). MyGeneLog™. https://www.mygenelog.com/variants/rs113907280

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