Sensitive

Rheumatoid arthritis (rheumatoid factor and/or anti-cyclic citrullinated peptide seropositive)

near BLTP1 · rs6814280

Where this position leads

Condition: Rheumatoid Arthritis

rs6814280 Condition: Rheumatoid Arthritis Rheumatoid Arthritis Condition rs6814280 rs6814280 near BLTP1

What the study found

Who was studied 17,221 European ancestry cases, 74,823 European ancestry controls, 8,340 East Asian ancestry cases, 162,608 East Asian ancestry controls, 841 African ancestry cases, 1,108 African ancestry controls, 689 South Asian ancestry cases, 1,258 South Asian ancestry controls, 357 Arab ancestry cases, 352 Arab ancestry controls.

The effect Each copy of the G allele carried 0.90 times the odds of Rheumatoid arthritis (rheumatoid factor and/or anti-cyclic citrullinated peptide seropositive) (95% confidence interval 0.866976576485334-0.933647164159003); p = 2 × 10−8.

Where it sits Chromosome 4, band 4q27 — between genes, 29.8 kb from BLTP1.

What each result means

A/A No copy of the version the research linked to Rheumatoid arthritis (rheumatoid factor and/or anti-cyclic citrullinated peptide seropositive). This is the starting point the study compared everyone against.
A/G One copy of the version the research linked to Rheumatoid arthritis (rheumatoid factor and/or anti-cyclic citrullinated peptide seropositive). That is a smaller link than two copies.
G/G Two copies of the version the research linked to Rheumatoid arthritis (rheumatoid factor and/or anti-cyclic citrullinated peptide seropositive). That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs6814280

What is rs6814280?

rs6814280 is a single position in the genome, in or near the near BLTP1 gene. Published research associates it with rheumatoid arthritis (rheumatoid factor and/or anti-cyclic citrullinated peptide seropositive). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs6814280 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 rs6814280 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 rs6814280 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 (rheumatoid factor and/or anti-cyclic citrullinated peptide seropositive) (rs6814280). MyGeneLog™. https://www.mygenelog.com/variants/rs6814280

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