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

near H2AL1Q · rs6527594

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Sensitive

Restless legs syndrome

near ALCAM · rs62262150

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Sensitive

Restless legs syndrome

near SLC32A1 · rs1322183

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Sensitive

Restless legs syndrome

near LINC01698 · rs12144563

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Sensitive

Restless legs syndrome

GPR139 · rs72772738

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Sensitive

Restless legs syndrome

PHACTR1 · rs9463138

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Sensitive

Restless legs syndrome

LINC01478 · rs35895933

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Sensitive

Restless legs syndrome

LINC01478 · rs12957682

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Sensitive

Restless legs syndrome

LINC02086 · rs3096648

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Sensitive

Restless legs syndrome

near LINC01717 · rs61815846

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Sensitive

Restless legs syndrome

near CAVIN3 · rs57325344

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Sensitive

Restless legs syndrome

R3HCC1L · rs61875279

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Sensitive

Restless legs syndrome

near PRPS1P1 · rs395961

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Sensitive

Restless legs syndrome

KCNMA1 · rs2116829

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Sensitive

Restless legs syndrome

DAB1 · rs1424470

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Sensitive

Restless legs syndrome

near UNC5B · rs72804595

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Sensitive

Restless legs syndrome

near RN7SKP212 · rs7638611

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Sensitive

Restless legs syndrome

SAMD5 · rs11155509

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Sensitive

Restless legs syndrome

PTPRD · rs1434253

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Sensitive

Restless legs syndrome

PARD3 · rs1415546

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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.