Variants linked to Parkinson's Disease

Continuously updated · newest added Oct 24, 2026

139 positions on this site are linked to Parkinson's Disease, out of 113,826 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

Mortality in Parkinson's disease

near RPL3 · rs12628329

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Sensitive

Parkinson's disease

TBC1D5 · rs1108439

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Sensitive

Parkinson's disease

near RNU6-471P · rs9393826

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Sensitive

Parkinson's disease

LAMP3 · rs71314284

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Sensitive

Parkinson's disease

SCARB2 · rs1550556

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Sensitive

Parkinson's disease

PLPP4 · rs12771445

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Sensitive

Parkinson's disease

near PHB1P21 · rs113487377

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Sensitive

Levodopa-induced dyskinesia in levodopa treated Parkinson's disease

GALNT14 · rs144125291

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Sensitive

Parkinson's disease-related grey matter volume atrophy

near SOCS2 · rs10859535

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Sensitive

Parkinson's disease

near FCGR2B · rs17411858

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Sensitive

Parkinson's disease

PITPNM2 · rs78299420

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Sensitive

Parkinson's disease

PIK3CA-DT · rs6806917

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Sensitive

Parkinson's disease-related grey matter volume atrophy

MOBP · rs1708104

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Sensitive

Parkinson's disease

near VN1R10P · rs9461359

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Sensitive

Parkinson's disease

HEATR6 · rs61204179

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Sensitive

Parkinson's disease

NOD2 · rs34133110

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Sensitive

Parkinson's disease

LINC01147 · rs1561758

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Sensitive

Parkinson's disease

ITGA2B · rs850731

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Sensitive

Parkinson's disease

LRRK2 · rs17443414

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Sensitive

Parkinson's disease

DCST1 · rs146143531

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Showing 20 of 139 · page 1 of 7

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.