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Restless legs syndrome (PheCode 327.71)

near LMO1 · rs7102266

Where this position leads

Condition: Restless Legs Syndrome

rs7102266 Condition: Restless Legs Syndrome Restless Legs Syndrome Condition rs7102266 rs7102266 near LMO1

What the study found

Who was studied 15,475 European ancestry cases, 428,445 European ancestry controls.

The effect Each copy of the C allele shifted the measure 0.108 lower (95% confidence interval 0.083-0.134); p = 2 × 10−17.

How common The C allele had a frequency of about 47% in the people studied.

Where it sits Chromosome 11, band 11p15.4 — between genes, 44.5 kb from LMO1.

What each result means

A/A No copy of the version the research linked to Restless legs syndrome (PheCode 327.71). This is the starting point the study compared everyone against.
A/C One copy of the version the research linked to Restless legs syndrome (PheCode 327.71). That is a smaller link than two copies.
C/C Two copies of the version the research linked to Restless legs syndrome (PheCode 327.71). That is the strongest link of the three results. A link in a study is not a diagnosis.
Source
Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program
Verma A, Huffman JE, Rodriguez A, Conery M, Liu M, Ho YL, Kim Y, Heise DA, Guare L, Panickan VA, Garcon H, Linares F
and 59 more — show all
Costa L, Goethert I, Tipton R, Honerlaw J, Davies L, Whitbourne S, Cohen J, Posner DC, Sangar R, Murray M, Wang X, Dochtermann DR, Devineni P, Shi Y, Nandi TN, Assimes TL, Brunette CA, Carroll RJ, Clifford R, Duvall S, Gelernter J, Hung A, Iyengar SK, Joseph J, Kember R, Kranzler H, Kripke CM, Levey D, Luoh SW, Merritt VC, Overstreet C, Deak JD, Grant SFA, Polimanti R, Roussos P, Shakt G, Sun YV, Tsao N, Venkatesh S, Voloudakis G, Justice A, Begoli E, Ramoni R, Tourassi G, Pyarajan S, Tsao P, O'Donnell CJ, Muralidhar S, Moser J, Casas JP, Bick AG, Zhou W, Cai T, Voight BF, Cho K, Gaziano JM, Madduri RK, Damrauer S, Liao KP
Science (New York, N.Y.) · 2024 · PMID 39024449 · open access

Questions about rs7102266

What is rs7102266?

rs7102266 is a single position in the genome, in or near the near LMO1 gene. Published research associates it with restless legs syndrome (phecode 327.71). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs7102266 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 rs7102266 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 rs7102266 come from?

GWAS Catalog, Science (New York, N.Y.) 2024, PMID:39024449. 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 (PheCode 327.71) (rs7102266). MyGeneLog™. https://www.mygenelog.com/variants/rs7102266

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