8,408 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.
NEURL1 · rs55693294
See detailed info → StandardHSF2 · rs9401451
See detailed info → StandardHAND2 · rs10520260
See detailed info → StandardPITX2 · rs138311480
See detailed info → StandardPITX2 · rs79399769
See detailed info → StandardPITX2 · rs6850025
See detailed info → StandardPITX2 · rs61501369
See detailed info → StandardKCNN3 · rs6689306
See detailed info → StandardLINC01426 · rs2834618
See detailed info → StandardMEX3C · rs8088085
See detailed info → StandardCYTH1 · rs12604076
See detailed info → StandardWNT3 · rs1563304
See detailed info → StandardZFHX3 · rs2359171
See detailed info → StandardRPL3L · rs140185678
See detailed info → StandardIGF1R · rs4965430
See detailed info → StandardARNT2 · rs12908004
See detailed info → StandardDPF3 · rs74884082
See detailed info → StandardSYNE2 · rs2738413
See detailed info → StandardCFL2 · rs73241997
See detailed info → StandardAKAP6 · rs11156751
See detailed info →Showing 20 of 8408 · page 410 of 421
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.