139 positions on this site are linked to Parkinson's Disease, out of 113,994 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.
TMEM163 · rs4954162
See detailed info → SensitiveRAB29 · rs11557080
See detailed info → SensitiveFGD4 · rs181609621
See detailed info → SensitiveKCNS3 · rs76116224
See detailed info → SensitiveALAS1 · rs143918452
See detailed info → SensitivePOLRMTP1 · rs148534175
See detailed info → SensitiveCAB39L · rs9568188
See detailed info → SensitiveCRHR1 · rs117615688
See detailed info → SensitiveCTSB · rs1293298
See detailed info → SensitiveGALC · rs979812
See detailed info → SensitiveVAMP4 · rs11578699
See detailed info → SensitiveDYRK1A · rs2248244
See detailed info → SensitiveUBTF · rs2269906
See detailed info → SensitiveCAMK2D · rs13117519
See detailed info → SensitiveSEMA4A · rs35643925
See detailed info → SensitiveZNF184 · rs9468199
See detailed info → SensitiveCHRNB1 · rs12600861
See detailed info → SensitiveTPM1 · rs117267308
See detailed info → SensitiveLHFPL2 · rs344650
See detailed info → SensitiveGPR65 · rs8005172
See detailed info →Showing 20 of 139 · page 6 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.