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

NFE2L1-DT · rs1468270

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Sensitive

Restless legs syndrome

near HLA-DRB9 · rs9269190

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Sensitive

Restless legs syndrome

near MTATP6P14 · rs4603157

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Sensitive

Restless legs syndrome (PheCode 327.71)

PTPRD · rs10116689

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Sensitive

Restless legs syndrome

OR5AU1 · rs10498276

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Sensitive

Restless legs syndrome

MDGA1 · rs708023

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Sensitive

Restless legs syndrome

LINC02520 · rs9369006

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Sensitive

Restless legs syndrome

CCDC148 · rs77276698

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Sensitive

Restless legs syndrome

LINC01249 · rs10193366

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Sensitive

Restless legs syndrome

CADM1 · rs11602686

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Sensitive

Restless legs syndrome

near LINGO2 · rs10757843

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Sensitive

Restless legs syndrome

near MICALL2 · rs113230729

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Sensitive

Restless legs syndrome (PheCode 327.71)

near LMO1 · rs7102266

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Sensitive

Restless legs syndrome

near ZBTB43 · rs537670230

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Sensitive

Restless legs syndrome

SLC26A5-AS1 · rs10233848

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Sensitive

Restless legs syndrome

MAP2K5 · rs1026732

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Sensitive

Restless legs syndrome in migraine without aura

near PMCH · rs76770509

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Sensitive

Restless legs syndrome

ATP2C1 · rs35987657

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Sensitive

Restless legs syndrome

RNF8 · rs17636328

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Sensitive

Restless legs syndrome

PTPRD · rs1975197

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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.