8,085 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.
LOC286083 · 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 → SensitiveHMGA2 · rs2261181
See detailed info → SensitiveFTO · rs9936385
See detailed info → SensitiveWFS1 · rs4458523
See detailed info → StandardFAM3C · rs798943
See detailed info → StandardWNT4 · rs2235529
See detailed info → StandardTNFSF11 · rs17536328
See detailed info → SensitiveADCY5 · rs11717195
See detailed info →Showing 20 of 8085 · page 298 of 405
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.