51 positions on this site are linked to Alzheimer's Disease Risk (APOE), out of 103,526 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.
PLEKHA1 · rs7908662
See detailed info → Sensitivenear LINC02838 · rs6978419
See detailed info → SensitiveMRC1 · rs4748424
See detailed info → SensitiveDENND3 · rs372758
See detailed info → SensitiveTPCN1 · rs6489896
See detailed info → SensitiveSYNPR · rs116668122
See detailed info → SensitiveOARD1 · rs10947943
See detailed info → Sensitivenear KIAA2013 · rs6682554
See detailed info → SensitiveBIN1 · rs35114168
See detailed info → SensitivePRICKLE1 · rs896559
See detailed info → SensitiveDIO2-AS1 · rs7155666
See detailed info → SensitiveZFYVE1 · rs182804071
See detailed info → Sensitivenear BIN1 · rs6431220
See detailed info → SensitiveAPOE · rs72654463
See detailed info → SensitiveAPOE · rs72654461
See detailed info → SensitiveFERMT2 · rs74825460
See detailed info → SensitiveLEF1-AS1 · rs34710518
See detailed info → SensitiveSNX1 · rs3848143
See detailed info → SensitiveTOMM40 · rs115908094
See detailed info → SensitiveOSBP2 · rs3804082
See detailed info →Showing 20 of 51 · page 1 of 3
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.