97,696 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.
CYP2C19 · rs7915414
See detailed info → StandardCYP2C19 · rs58667319
See detailed info → StandardCYP2C19 · rs9888067
See detailed info → SensitiveCYP2C19 · rs57991629
See detailed info → SensitiveCYP2C19 · rs116855710
See detailed info → SensitiveCYP2C19 · rs4244285
See detailed info → SensitiveCYP2C19 · rs4986893
See detailed info → StandardCYP2C19 · rs12248560
See detailed info → StandardCYP2C19 · rs35013847
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.