102,854 variants MyGeneLog™ checks for — each with its own plain-language page and cited source. New findings are collected from the public GWAS Catalog every twenty minutes.
NECTIN2 · rs8105340
See detailed info → SensitiveZNF594-DT · rs58124010
See detailed info → SensitiveSORL1 · rs74685827
See detailed info → Standardnear CBLC · rs117142879
See detailed info → StandardAPOC1 · rs72654445
See detailed info → StandardNECTIN2 · rs187183066
See detailed info → SensitiveZNF594-DT · rs7225151
See detailed info → SensitiveTSPAN14 · rs6586028
See detailed info → SensitiveCD2AP · rs7767350
See detailed info → Standard on its ownnear APOE · rs1081106
See detailed info → StandardCBLC · rs139425456
See detailed info → Sensitivenear HLA-DQA1 · rs6605556
See detailed info → StandardBCAM · rs180887453
See detailed info → Sensitivenear RNU6-560P · rs3851179
See detailed info → Sensitivenear MIR4280HG · rs62374257
See detailed info → StandardGEMIN7 · rs78620885
See detailed info → Standard on its ownnear APOE · rs72654473
See detailed info → SensitiveAPOE · rs405509
See detailed info → SensitiveAPOE · rs769450
See detailed info → StandardAPOE · rs115299243
See detailed info →Showing 20 of 81 · page 3 of 5
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.