103,190 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.
near CYP2A6 · rs2259217
See detailed info → StandardCYP2A6 · rs117287096
See detailed info → Standard on its ownnear CYP2A6 · rs556743951
See detailed info → Standard on its ownnear CYP2A6 · rs145580088
See detailed info → Sensitivenear CYP2A6 · rs4803381
See detailed info → StandardCYP2A6 · rs8192726
See detailed info → StandardCYP2A6 · rs28399462
See detailed info → StandardCYP2A6 · rs55921593
See detailed info → StandardCYP2A6 · rs150586234
See detailed info → StandardCYP2A6 · rs56267346
See detailed info → StandardCYP2A6 · rs1801272
See detailed info → StandardCYP2A6 · rs12459249
See detailed info → StandardCYP2A6 · rs184589612
See detailed info → StandardCYP2A6 · rs66500423
See detailed info → StandardCYP2A6 · rs7247903
See detailed info → StandardCYP2A6 · rs113029345
See detailed info → StandardCYP2A6 · rs56113850
See detailed info → StandardCYP2A6 · rs4105144
See detailed info →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.