12,469 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.
ANUBL1 · rs2279434
See detailed info → StandardCNNM2 · rs12413409
See detailed info → StandardSOX17 · rs9298506
See detailed info → SensitiveLRRK2 · rs1491942
See detailed info → SensitiveGAK · rs6599388
See detailed info → StandardIRF1 · rs4705952
See detailed info → StandardOAS3 · rs2072134
See detailed info → StandardMYL2 · rs12229654
See detailed info → StandardSPIB · rs3745516
See detailed info → StandardPTPN2 · rs2847281
See detailed info → StandardFOXO1 · rs2755237
See detailed info → Standardnear GOLGA8M · rs8033165
See detailed info → SensitiveCMYC · rs10088218
See detailed info → SensitiveBUD13 · rs11820589
See detailed info → StandardCETP · rs173539
See detailed info → StandardFADS1 · rs174547
See detailed info → Standard on its ownABO · rs579459
See detailed info → Standard on its ownSCGN · rs742132
See detailed info → SensitiveREL · rs13017599
See detailed info → SensitiveMHC · rs13194053
See detailed info →Showing 20 of 12469 · page 588 of 624
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.