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.
PLG · rs783147
See detailed info → SensitiveMHC · rs4248154
See detailed info → SensitiveMHC · rs4313034
See detailed info → SensitiveMHC · rs3893464
See detailed info → Standard on its ownLPAL2 · rs12214416
See detailed info → SensitiveSYK · rs290227
See detailed info → Standard on its ownTNS3 · rs700752
See detailed info → StandardINHBC · rs1106766
See detailed info → StandardABO · rs612169
See detailed info → StandardPCSK9 · rs2479409
See detailed info → StandardSLC2A9 · rs4481233
See detailed info → StandardCYP3A4 · rs17277546
See detailed info → StandardSCD · rs603424
See detailed info → StandardOPLAH · rs6558295
See detailed info → StandardIL12B · rs2546890
See detailed info → SensitiveHLA-C · rs13191343
See detailed info → Standard on its ownGCFC2 · rs2298948
See detailed info → StandardLPL · rs10105606
See detailed info → Standard on its ownCELSR2 · rs7528419
See detailed info → Standard on its ownLDLR · rs6511720
See detailed info →Showing 20 of 12469 · page 576 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.