566 positions on this site are linked to Alzheimer's Disease, out of 118,864 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.
KALRN · rs1375566941
See detailed info → Sensitivenear TEX44 · rs1375871492
See detailed info → SensitiveECHDC2 · rs1376370722
See detailed info → SensitiveCOLQ · rs1378323638
See detailed info → Sensitivenear BRSK2 · rs1379529633
See detailed info → Sensitivenear XRCC2 · rs1385078687
See detailed info → Sensitivenear CKMT1A · rs1385582538
See detailed info → Sensitivenear WIPI2 · rs1388898746
See detailed info → SensitivePITPNC1 · rs1389719881
See detailed info → Sensitivenear USP12 · rs1392734500
See detailed info → Sensitivenear BCL3 · rs139326841
See detailed info → Sensitivenear CCNYL1B · rs1394896178
See detailed info → SensitiveEFCAB12 · rs1396035227
See detailed info → SensitiveCBLC · rs139997344
See detailed info → Sensitivenear APOC2 · rs141441332
See detailed info → Sensitivenear MED13 · rs1414985603
See detailed info → Sensitivenear EGFL7 · rs1417363683
See detailed info → Sensitivenear ETV1 · rs1421858724
See detailed info → Sensitivenear HECTD1 · rs142188527
See detailed info → SensitiveHACL1 · rs1424900334
See detailed info →Showing 20 of 566 · page 14 of 29
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.