Sensitive

Restless legs syndrome

PTPRD · rs4626664

Where this position leads

Condition: Restless Legs Syndrome

rs4626664 Condition: Restless Legs Syndrome Restless Legs Syndrome Condition rs4626664 rs4626664 PTPRD

What the study found

Who was studied 628 European ancestry cases, 1,644 European ancestry controls; replicated in 1,550 European ancestry cases, 2,269 European ancestry controls, 285 French Canadian founder cases, 842 French Canadian founder controls.

The effect Each copy of the A allele carried 1.44 times the odds of Restless legs syndrome (95% confidence interval 1.31-1.59); p = 6 × 10−10.

How common The A allele had a frequency of about 12% in the people studied.

Where it sits Chromosome 9, band 9p23 — in an intron of PTPRD.

What each result means

A/A Two copies of the version the research linked to Restless legs syndrome. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/G One copy of the version the research linked to Restless legs syndrome. That is a smaller link than two copies.
G/G No copy of the version the research linked to Restless legs syndrome. This is the starting point the study compared everyone against.
Source

Questions about rs4626664

What is rs4626664?

rs4626664 is a single position in the genome, in or near the PTPRD 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 rs4626664 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.

Does having rs4626664 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 rs4626664 come from?

GWAS Catalog, Nat Genet 2008, PMID:18660810. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.

Restless legs syndrome (rs4626664). MyGeneLog™. https://www.mygenelog.com/variants/rs4626664

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