Sensitive

Rheumatoid arthritis

near PTPRC · rs28398409

Where this position leads

Condition: Rheumatoid Arthritis

rs28398409 Condition: Rheumatoid Arthritis Rheumatoid Arthritis Condition rs28398409 rs28398409 near PTPRC

What the study found

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 0.91 times the odds of Rheumatoid arthritis (95% confidence interval 0.880170706428243-0.938980474185154); p = 8 × 10−9.

Where it sits Chromosome 1, band 1q31.3 — between genes, 15 kb from PTPRC.

What each result means

A/A No copy of the version the research linked to Rheumatoid arthritis. This is the starting point the study compared everyone against.
A/G One copy of the version the research linked to Rheumatoid arthritis. That is a smaller link than two copies.
G/G Two 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.
Source

Questions about rs28398409

What is rs28398409?

rs28398409 is a single position in the genome, in or near the near PTPRC 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 rs28398409 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 rs28398409 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 rs28398409 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.

Quoting this page

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Rheumatoid arthritis (rs28398409). MyGeneLog™. https://www.mygenelog.com/variants/rs28398409

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