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Who was studied 22,350 European ancestry cases, 74,823 European ancestry controls, 11,025 East Asian ancestry cases, 162,608 East Asian ancestry controls, 999 African ancestry cases, 1,108 African ancestry controls, 986 South Asian ancestry cases, 1,258 South Asian ancestry controls, 511 Arab ancestry cases, 352 Arab ancestry controls.
The effect
Each copy of the G allele carried 1.09 times the odds of Rheumatoid arthritis (95% confidence interval 1.06150387618034-1.1186221561566); p = 1 × 10−10.
Where it sits Chromosome 1, band 1q21.3 — in an intron of IL6R.
What each result means
C/CNo copy of the version the research linked to Rheumatoid arthritis. This is the starting point the study compared everyone against.
C/GOne copy of the version the research linked to Rheumatoid arthritis. That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Rheumatoid arthritis. That is the strongest link of the three results. A link in a study is not a diagnosis.
rs4341355 is a single position in the genome, in or near the IL6R gene. Published research associates it with rheumatoid arthritis. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs4341355 linked to?
On MyGeneLog this position is linked to Rheumatoid Arthritis. The research behind each link, and its sources, are set out on that condition page.
Does having rs4341355 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 rs4341355 come from?
GWAS Catalog, Nature genetics 2022, PMID:36333501. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
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