Variants linked to Restless Legs Syndrome

Continuously updated · newest added Oct 21, 2026

112 positions on this site are linked to Restless Legs Syndrome, out of 102,896 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

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Sensitive

Restless legs syndrome

FRMD4A · rs12218808

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Sensitive

Restless legs syndrome

PDE9A · rs36098823

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Sensitive

Restless legs syndrome

LRRTM4 · rs115436562

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Sensitive

Restless legs syndrome

STK33 · rs73402082

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Sensitive

Restless legs syndrome

near LINC00276 · rs2380524

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Sensitive

Restless legs syndrome

near CYB5AP5 · rs8021157

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Sensitive

Restless legs syndrome

near CAVIN3 · rs10839553

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Sensitive

Restless legs syndrome

near LINC01717 · rs61815845

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Sensitive

Restless legs syndrome (PheCode 327.71)

near LINC01304 · rs1908245

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Sensitive

Restless legs syndrome

XKR6 · rs4451266

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Sensitive

Restless legs syndrome

near TACSTD2 · rs232822

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Sensitive

Restless legs syndrome

DAB1 · rs12565446

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Sensitive

Restless legs syndrome

ENOX1 · rs4942239

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Sensitive

Restless legs syndrome

PTPRD · rs76276550

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Sensitive

Restless legs syndrome

near UNC5B · rs7099994

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Sensitive

Restless legs syndrome

CCDC148 · rs199997012

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Sensitive

Restless legs syndrome

ACTN1 · rs730635

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Sensitive

Restless legs syndrome

near SEMA6D · rs192695785

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Sensitive

Restless legs syndrome (PheCode 327.71)

CCDC148 · rs145834406

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Sensitive

Restless legs syndrome

PTPRD · rs10758996

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Questions about variants on this site

What is a "variant" page on this site?

One specific position in the genome (an rsID), explained in plain language with what published research has found it linked to, and how strong that link actually is.

Where does new variant data come from?

The public GWAS Catalog, checked every twenty minutes, plus variants added manually after research review. Every one passes the same quality gate before publishing.

Does being listed here mean a variant causes a condition?

No. Listing reflects an association from published research, not a diagnosis or a cause. Most common variants shift probability modestly rather than determining an outcome.

Can I search this list by gene or rsID?

Yes — the search box above matches gene symbols and rsIDs as well as trait names.