12,423 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.
COLEC10 · rs2450083
See detailed info → StandardWNT4 · rs3920498
See detailed info → StandardLITAF · rs12930096
See detailed info → StandardLITAF · rs12444261
See detailed info → Sensitive on its ownLINC00928 · rs8038108
See detailed info → StandardCDHR3 · rs6967330
See detailed info → StandardC5orf56 · rs2106854
See detailed info → StandardRUNX1 · rs8128234
See detailed info → Standard on its ownBCHE · rs6445035
See detailed info → StandardIFIH1 · rs3747517
See detailed info → StandardREL · rs842625
See detailed info → StandardIL12B · rs7709212
See detailed info → StandardCOG6 · rs34394770
See detailed info → StandardGDF5 · rs224333
See detailed info → StandardDLEU7 · rs3118906
See detailed info → StandardMTMR11 · rs11205303
See detailed info → StandardAMZ1 · rs798554
See detailed info → StandardH6PD · rs6662509
See detailed info → StandardBMP6 · rs1885486
See detailed info → StandardACAN · rs2280470
See detailed info →Showing 20 of 12423 · page 530 of 622
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.