12,469 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.
MPP7 · rs3905706
See detailed info → Standard on its ownGGT1 · rs4820599
See detailed info → StandardLEKR1 · rs344081
See detailed info → StandardHMGCR · rs7703051
See detailed info → Standard on its ownBCO2 · rs1834481
See detailed info → StandardLCORL · rs7678436
See detailed info → StandardPLCB4 · rs2072910
See detailed info → Standard on its ownGCKR · rs780094
See detailed info → SensitiveTRAF1 · rs1953126
See detailed info → SensitiveUBE2L3 · rs2298428
See detailed info → SensitiveELMO1 · rs11984075
See detailed info → StandardSIRPA · rs6136489
See detailed info → StandardFGB · rs1800789
See detailed info → StandardCOL5A1 · rs3132306
See detailed info → SensitivePPAP2B · rs17114036
See detailed info → Standard on its ownXPNPEP1 · rs17095355
See detailed info → StandardMC4R · rs12970134
See detailed info → Standard on its ownICAM1 · rs5498
See detailed info → Standard on its ownTYRP1 · rs1408799
See detailed info → StandardNRXN3 · rs10146997
See detailed info →Showing 20 of 12469 · page 584 of 624
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.