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.
TMEM175 · rs34884217
See detailed info → SensitiveSH3GL2 · rs10756907
See detailed info → SensitiveLOC100131289 · rs4140646
See detailed info → SensitiveSNCA · rs5019538
See detailed info → SensitiveMCCC1 · rs140278703
See detailed info → SensitiveHASPIN · rs11653889
See detailed info → SensitiveDNAH17 · rs666463
See detailed info → SensitiveWNT3 · rs199501
See detailed info → SensitiveSPTSSB · rs1450522
See detailed info → SensitiveMUC12 · rs78837976
See detailed info → SensitiveSNCA · rs356228
See detailed info → SensitiveCLCN3 · rs62333164
See detailed info → SensitiveSATB1 · rs73038319
See detailed info → SensitiveFAM47E-STBD1 · rs6854006
See detailed info → SensitiveCRHR1 · rs62053943
See detailed info → SensitiveMIPOL1 · rs12147950
See detailed info → SensitiveKPNA1 · rs55961674
See detailed info → SensitiveFAM49B · rs2086641
See detailed info → SensitiveLRRK2 · rs117073808
See detailed info → SensitiveMED12L · rs11707416
See detailed info →Showing 20 of 139 · page 5 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.