UTC
Sensitive

Rheumatoid arthritis

CCL19 · rs11574914

Where this position leads

Condition: Rheumatoid Arthritis

rs11574914 Condition: Rheumatoid Arthritis Rheumatoid Arthritis Condition rs11574914 rs11574914 CCL19

What each result means

A/A Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Rheumatoid arthritis compared to the general population. (GWAS Catalog, Nature 2013, PMID:24390342)
A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Rheumatoid arthritis. (GWAS Catalog, Nature 2013, PMID:24390342)
G/G Published research associates this genotype with typical/baseline likelihood of Rheumatoid arthritis — no copies of the reported risk allele. (GWAS Catalog, Nature 2013, PMID:24390342)

Source: GWAS Catalog, Nature 2013, PMID:24390342

What people read about alongside this

Bones and fractures1

Papers in Europe PMC whose title or abstract names both this rsID and that subject. A shared paper means somebody wrote about the two together — it is not a claim that this position explains the subject.

Questions about rs11574914

What is rs11574914?

rs11574914 is a single position in the genome, in or near the CCL19 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 rs11574914 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.

What do people read about alongside rs11574914?

Subjects that appear in the title or abstract of the same papers as this rsID include bones and fractures (1 papers). A shared paper means somebody wrote about the two together; it is not a claim that this position explains the topic.

Does having rs11574914 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 rs11574914 come from?

GWAS Catalog, Nature 2013, PMID:24390342. 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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