8,787 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.
CDCA7 · rs10930597
See detailed info → StandardGPR146 · rs1997243
See detailed info → Standard on its ownCYP19A1 · rs2414095
See detailed info → StandardPLEKHG1 · rs17080102
See detailed info → StandardCBX7 · rs877529
See detailed info → SensitiveADAM15 · rs1218582
See detailed info → SensitiveTBX5 · 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 →Showing 20 of 8787 · page 321 of 440
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.