10,938 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.
TNPO3 · rs12537284
See detailed info → SensitiveLPL · rs2083637
See detailed info → StandardWDR72 · rs17730281
See detailed info → StandardLRP1B · rs2890652
See detailed info → StandardNOS2 · rs4795067
See detailed info → StandardNFE2L3 · rs1055144
See detailed info → StandardNISCH · rs6784615
See detailed info → SensitiveTMEM129 · rs798766
See detailed info → StandardBCAS3 · rs11868441
See detailed info → SensitiveTERT · rs2736100
See detailed info → StandardHBS1L · rs9399137
See detailed info → Standard on its ownBMF · rs4924410
See detailed info → Standard on its ownTARDBP · rs9430161
See detailed info → Standard on its ownLYPLAL1 · rs11118316
See detailed info → Standard on its ownCHRNA5 · rs2036527
See detailed info → Standard on its ownTNFRSF13B · rs4792800
See detailed info → Standard on its ownESR1 · rs12173570
See detailed info → StandardENPEP · rs6825911
See detailed info → StandardSLC2A9 · rs11722228
See detailed info → StandardABCG2 · rs4148155
See detailed info →Showing 20 of 10938 · page 497 of 547
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.