8,812 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.
IL6R · rs61812598
See detailed info → Standard on its ownCBS · rs6586282
See detailed info → Standard on its ownHOMER1 · rs6859667
See detailed info → Standard on its ownARSB · rs17823744
See detailed info → Standard on its ownAREG · rs12642133
See detailed info → SensitiveZNF438 · rs793108
See detailed info → Standard on its ownANO3 · rs114444506
See detailed info → StandardLOC286083 · rs28680850
See detailed info → SensitiveSFTPD · rs726288
See detailed info → SensitivePVT1 · rs1516971
See detailed info → StandardCCR6 · rs62436827
See detailed info → StandardSIK3 · rs139961185
See detailed info → Standard on its ownPDGFRA · rs1800813
See detailed info → SensitiveBCKDK · rs14235
See detailed info → Standard on its ownnear SI · rs2168784
See detailed info → SensitiveVPS13C · rs2414739
See detailed info → SensitiveTMEM229B · rs1555399
See detailed info → Standard on its ownCMPK1 · rs17103186
See detailed info → StandardFAM3C · rs7776725
See detailed info → SensitiveZMIZ1 · rs12571751
See detailed info →Showing 20 of 8812 · page 334 of 441
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.