Variants linked to Restless Legs Syndrome

Continuously updated · newest added Oct 21, 2026

113 positions on this site are linked to Restless Legs Syndrome, out of 103,064 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

LINC02497 · rs6811899

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Sensitive

Restless legs syndrome

near PPM1AP1 · rs2736019

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Sensitive

Restless legs syndrome

near GAPDHP56 · rs13104564

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Sensitive

Restless legs syndrome

ADGRB3 · rs779452

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Sensitive

Restless legs syndrome

RIMS2 · rs56146220

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Sensitive

Restless legs syndrome

near PBX3 · rs4838313

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Sensitive

Restless legs syndrome

LINC00470 · rs4797688

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Sensitive

Restless legs syndrome

near LINC01680 · rs12065220

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Sensitive

Restless legs syndrome

TRPM3 · rs768694

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Sensitive

Restless legs syndrome

near PBX3 · rs7029545

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Sensitive

Restless legs syndrome

near MTND4P3 · rs6971845

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Sensitive

Restless legs syndrome

CDH4 · rs6121424

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Sensitive

Restless legs syndrome

PPP2R5C · rs1741142

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Sensitive

Restless legs syndrome

near LINC00276 · rs1510825

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Sensitive

Restless legs syndrome

near COPS5P1 · rs1324118

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Sensitive

Restless legs syndrome

DIAPH3 · rs11838906

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Sensitive

Restless legs syndrome

near NAMPTP2 · rs166609

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Sensitive

Restless legs syndrome

near RAC1P8 · rs4886357

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Sensitive

Restless legs syndrome

DAB1 · rs3738555

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Sensitive

Restless legs syndrome

PDE9A · rs28842577

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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.