12,424 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.
SMAD3 · rs17294280
See detailed info → StandardZBTB10 · rs7009110
See detailed info → StandardCLEC16A · rs62026376
See detailed info → StandardBACH2 · rs10944479
See detailed info → StandardG6PC2 · rs3755157
See detailed info → StandardTAOK3 · rs6490177
See detailed info → StandardLHX2 · rs2075064
See detailed info → StandardSEMA6D · rs12442330
See detailed info → StandardDCAF5 · rs1275411
See detailed info → StandardNOS1 · rs3741475
See detailed info → StandardIGSF9B · rs167915
See detailed info → StandardCNTN5 · rs10790767
See detailed info → Standardnear CREB3L1 · rs12283653
See detailed info → Standardnear BMAL1 · rs4757136
See detailed info → StandardPTCH1 · rs75614054
See detailed info → Standardnear MBNL2 · rs9516861
See detailed info → StandardFAM120A · rs78046549
See detailed info → SensitiveCHADL · rs9607782
See detailed info → StandardFN3K · rs1046875
See detailed info → StandardGNMT · rs9296404
See detailed info →Showing 20 of 12424 · page 524 of 622
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.