51 positions on this site are linked to Alzheimer's Disease Risk (APOE), out of 103,358 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.
TREML2 · rs9394766
See detailed info → Sensitivenear RNU6-560P · rs1898895
See detailed info → SensitiveLNCOB1 · rs166907
See detailed info → SensitiveSORL1 · rs117807585
See detailed info → SensitiveAPOE · rs435380
See detailed info → SensitiveAPOE · rs446037
See detailed info → Sensitivenear TREML2 · rs60755019
See detailed info → SensitiveLINC01234 · rs111486601
See detailed info → SensitiveNECTIN2 · rs8105340
See detailed info → SensitiveZNF594-DT · rs58124010
See detailed info → SensitiveSORL1 · rs74685827
See detailed info → SensitiveZNF594-DT · rs7225151
See detailed info → SensitiveTSPAN14 · rs6586028
See detailed info → SensitiveCD2AP · rs7767350
See detailed info → Sensitivenear HLA-DQA1 · rs6605556
See detailed info → Sensitivenear RNU6-560P · rs3851179
See detailed info → Sensitivenear MIR4280HG · rs62374257
See detailed info → StandardTOMM40 · rs34095326
See detailed info → StandardAPOC1 · rs12721046
See detailed info → StandardTOMM40 · rs71352238
See detailed info →Showing 20 of 51 · page 2 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.