8,721 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.
TBX5 · rs1270884
See detailed info → SensitiveNGFR · rs11650494
See detailed info → SensitiveLACE1 · rs2273669
See detailed info → SensitiveMCM3AP · rs2839186
See detailed info → StandardPOLB · rs3136739
See detailed info → Standard on its ownHTR3D · rs1401999
See detailed info → Standard on its ownSOX9 · rs12946942
See detailed info → Standard on its ownnear SFRP2 · rs13135284
See detailed info → StandardHDGF · rs12145743
See detailed info → StandardPTPRJ · rs138315285
See detailed info → StandardMYBPC3 · rs2856656
See detailed info → StandardTAOK1 · rs9900280
See detailed info → Standard on its ownDEFAs · rs2738048
See detailed info → SensitiveETS1 · rs73013527
See detailed info → StandardFAM155E · rs11796357
See detailed info → SensitiveIL20RB · rs9826828
See detailed info → Standard on its ownnear CD34 · rs1318653
See detailed info → Standard on its ownIFI44L · rs273259
See detailed info → Standard on its ownSCN2A · rs3769955
See detailed info → Standard on its ownnear ATP2B1 · rs11105468
See detailed info →Showing 20 of 8721 · page 318 of 437
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.