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.
near GPRIN3 · rs114762839
See detailed info → SensitiveFMNL1-DT · rs62066707
See detailed info → SensitiveMED12L · rs6803771
See detailed info → SensitiveARHGAP27 · rs8327
See detailed info → SensitiveSPATA6 · rs1311506805
See detailed info → Sensitivenear TPRA1 · rs559557961
See detailed info → Sensitivenear MUC19 · rs11177328
See detailed info → SensitiveLDLRAD4 · rs73415968
See detailed info → SensitiveCOMMD1 · rs528521148
See detailed info → Sensitivenear RNA5SP102 · rs145533835
See detailed info → Sensitivenear H2ACP1 · rs368657122
See detailed info → SensitiveDLG2 · rs6592142
See detailed info → SensitiveSV2C · rs246815
See detailed info → Sensitivenear CCSER1 · rs78327649
See detailed info → Sensitivenear Y_RNA · rs4421827
See detailed info → SensitiveCNTN1 · rs1442190
See detailed info → SensitiveCCT3 · rs35161831
See detailed info → SensitiveWDHD1 · rs8018800
See detailed info → SensitiveMMRN1 · rs79214011
See detailed info → SensitiveCNTN1 · rs73273590
See detailed info →Showing 20 of 139 · page 2 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.