Sensitive

Osteoarthritis

near PRDM5 · rs11729628

Where this position leads

Condition: Knee Osteoarthritis

rs11729628 Condition: Knee Osteoarthritis Knee Osteoarthritis Condition rs11729628 rs11729628 near PRDM5

What the study found

Who was studied 175,803 European ancestry cases, 644,862 European ancestry controls, 1,265 Japanese ancestry cases, 449 Southern Chinese ancestry cases, 3,330 Japanese ancestry controls, 981 Southern Chinese ancestry controls.

The effect Each copy of the T allele carried 0.97 times the odds of Osteoarthritis (95% confidence interval 0.959169178-0.979304953); p = 5 × 10−9.

How common The T allele had a frequency of about 24% in the people studied.

Where it sits Chromosome 4, band 4q27 — between genes, 21.8 kb from PRDM5.

What each result means

G/G No copy of the version the research linked to Osteoarthritis. This is the starting point the study compared everyone against.
G/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 rs11729628

What is rs11729628?

rs11729628 is a single position in the genome, in or near the near PRDM5 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 rs11729628 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 rs11729628 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 rs11729628 come from?

GWAS Catalog, Cell 2021, PMID:34450027. 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 (rs11729628). MyGeneLog™. https://www.mygenelog.com/variants/rs11729628

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