Sensitive

Restless legs syndrome

BTBD9 · rs3923809

Where this position leads

Condition: Restless Legs Syndrome

rs3923809 Condition: Restless Legs Syndrome Restless Legs Syndrome Condition rs3923809 rs3923809 BTBD9

What each result means

A/A Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Restless legs syndrome compared to the general population. (GWAS Catalog, N Engl J Med 2007, PMID:17634447)
A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Restless legs syndrome. (GWAS Catalog, N Engl J Med 2007, PMID:17634447)
G/G Published research associates this genotype with typical/baseline likelihood of Restless legs syndrome — no copies of the reported risk allele. (GWAS Catalog, N Engl J Med 2007, PMID:17634447)

Source: GWAS Catalog, N Engl J Med 2007, PMID:17634447

What people read about alongside this

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 rs3923809

What is rs3923809?

rs3923809 is a single position in the genome, in or near the BTBD9 gene. Published research associates it with restless legs syndrome. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs3923809 linked to?

On MyGeneLog this position is linked to Restless Legs Syndrome. The research behind each link, and its sources, are set out on that condition page.

What do people read about alongside rs3923809?

Subjects that appear in the title or abstract of the same papers as this rsID include adhd and attention (1 papers), sleep and insomnia (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 rs3923809 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 rs3923809 come from?

GWAS Catalog, N Engl J Med 2007, PMID:17634447. 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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