Sensitive

Rheumatoid arthritis

CCR6 · rs1854853

Where this position leads

Condition: Rheumatoid Arthritis

rs1854853 Condition: Rheumatoid Arthritis Rheumatoid Arthritis Condition rs1854853 rs1854853 CCR6

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.
A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Rheumatoid arthritis.
G/G Published research associates this genotype with typical/baseline likelihood of Rheumatoid arthritis — no copies of the reported risk allele.
Source

Questions about rs1854853

What is rs1854853?

rs1854853 is a single position in the genome, in or near the CCR6 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 rs1854853 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 rs1854853 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 rs1854853 come from?

GWAS Catalog, Arthritis Rheumatol 2014, PMID:24782177. 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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