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.
CCDC62 · rs11060180
See detailed info → SensitiveLRRK2 · rs76904798
See detailed info → SensitiveGPNMB · rs199347
See detailed info → SensitiveINPP5F · rs117896735
See detailed info → SensitiveHLA-DQB · rs9275326
See detailed info → SensitiveTMEM175 · rs34311866
See detailed info → SensitiveSIPA1L2 · rs10797576
See detailed info → SensitiveSTK39 · rs1474055
See detailed info → SensitiveGBA · rs35749011
See detailed info → SensitiveVPS13C · rs2414739
See detailed info → SensitiveBCKDK · rs14235
See detailed info → SensitiveTMEM229B · rs1555399
See detailed info → SensitiveLRRK2 · rs34637584
See detailed info → SensitiveSCARB2 · rs6812193
See detailed info → SensitiveMCCC1 · rs11711441
See detailed info → SensitiveSNCA · rs356219
See detailed info → SensitiveLRRK2 · rs1491942
See detailed info → SensitiveGAK · rs6599388
See detailed info → SensitiveMAPT · rs393152
See detailed info →Showing 19 of 139 · page 7 of 7
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.
The public GWAS Catalog, checked every twenty minutes, plus variants added manually after research review. Every one passes the same quality gate before publishing.
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.
Yes — the search box above matches gene symbols and rsIDs as well as trait names.