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 113,825 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

Parkinson's disease

near SNCA · rs79483792

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Sensitive

Parkinson's disease

GAK · rs75072999

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Sensitive

Parkinson's disease

LRRK2 · rs34594498

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Sensitive

Parkinson's disease

near SEC23IP · rs118117788

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Sensitive

Parkinson's disease

CCSER1 · rs75541595

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Sensitive

Parkinson's disease

SLC2A13 · rs28370650

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Sensitive

Parkinson's disease

HMGN2P18 · rs35682329

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Sensitive

Parkinson's disease-related grey matter volume atrophy

MBP · rs470934

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Sensitive

Parkinson's disease

SLC18B1 · rs41286192

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Sensitive

Parkinson's disease

ASH1L · rs12734374

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Sensitive

Parkinson's disease

ITPKB · rs4653767

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Sensitive

Parkinson's disease

MCCC1 · rs140278703

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Sensitive

Parkinson's disease or first degree relation to individual with Parkinson's disease

LOC100131289 · rs4140646

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Sensitive

Parkinson's disease or first degree relation to individual with Parkinson's disease

SH3GL2 · rs10756907

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Sensitive

Parkinson's disease

TMEM175 · rs34884217

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Sensitive

Parkinson's disease or first degree relation to individual with Parkinson's disease

CD19 · rs2904880

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Sensitive

Parkinson's disease or first degree relation to individual with Parkinson's disease

GXYLT1 · rs144755950

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Sensitive

Parkinson's disease

KANSL1 · rs113564729

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Sensitive

Parkinson's disease

RP11-162I7 · rs3889108

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Sensitive

Parkinson's disease

STX1B · rs140820592

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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.