12,426 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.
CWC27 · rs7731168
See detailed info → StandardNR3C2 · rs6535594
See detailed info → StandardSHROOM3 · rs7654754
See detailed info → StandardPRKCI · rs112607182
See detailed info → StandardMYL3 · rs6768627
See detailed info → StandardSPHKAP · rs35924503
See detailed info → StandardCEND1 · rs7117921
See detailed info → Standard on its ownCCNL1 · rs1482853
See detailed info → StandardMEF2C · rs11951031
See detailed info → SensitiveABCA7 · rs115550680
See detailed info → StandardPOU2AF1 · rs4938534
See detailed info → Standard on its ownMICAL3 · rs1076540
See detailed info → Standard on its ownMLIP · rs9296736
See detailed info → StandardTRPS1 · rs2737229
See detailed info → Standard on its ownKCNJ6 · rs2835872
See detailed info → SensitiveTEC · rs2664035
See detailed info → SensitiveTNFAIP3 · rs7752903
See detailed info → StandardLRRN2 · rs3789044
See detailed info → SensitiveHLA region · rs6935723
See detailed info → StandardASB18 · rs13401104
See detailed info →Showing 20 of 12426 · page 511 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.