Sensitive

Knee osteoarthritis

SPHKAP · rs11685283

Where this position leads

Condition: Knee Osteoarthritis

rs11685283 Condition: Knee Osteoarthritis Knee Osteoarthritis Condition rs11685283 rs11685283 SPHKAP

What the study found

Who was studied 161,228 European ancestry cases, 965,985 European ancestry controls, 5,433 East Asian ancestry cases, 126,769 East Asian ancestry controls, 3,463 African or African American cases, 21,448 African or African American controls, 993 South Asian ancestry cases, 18,871 South Asian ancestry controls, 523 Hispanic cases, 2,903 Hispanic controls, 616 Admixed ancestry cases, 8,268 Admixed ancestry controls.

The effect Each copy of the T allele carried 1.03 times the odds of Knee osteoarthritis (95% confidence interval 1.01731637091237-1.03420379326642); p = 2 × 10−9.

How common The T allele had a frequency of about 57% in the people studied.

Where it sits Chromosome 2, band 2q36.3 — in an intron of SPHKAP.

What each result means

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

Questions about rs11685283

What is rs11685283?

rs11685283 is a single position in the genome, in or near the SPHKAP gene. Published research associates it with knee 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 rs11685283 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 rs11685283 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 rs11685283 come from?

GWAS Catalog, Nature 2025, PMID:40205036. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

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Knee osteoarthritis (rs11685283). MyGeneLog™. https://www.mygenelog.com/variants/rs11685283

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