7,431 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.
LRP1B · rs116792882
See detailed info → StandardMRPS14 · rs6669560
See detailed info → StandardCWC27 · rs7731168
See detailed info → StandardNR3C2 · rs6535594
See detailed info → StandardSHROOM3 · rs7654754
See detailed info → StandardPRKCI · rs112607182
See detailed info → StandardMYL3 · rs6768627
See detailed info → StandardACTL7B · rs2417930
See detailed info → StandardSPHKAP · rs35924503
See detailed info → StandardATP1B1 · rs1200108
See detailed info → StandardTRIB1 · rs28601761
See detailed info → StandardWIPF3 · rs17158386
See detailed info → SensitiveABCA7 · rs115550680
See detailed info → Standard on its ownCCNL1 · rs1482853
See detailed info → StandardMEF2C · rs11951031
See detailed info → Standard on its ownMLIP · rs9296736
See detailed info → StandardPOU2AF1 · rs4938534
See detailed info → Standard on its ownMICAL3 · rs1076540
See detailed info → Standard on its ownKCNJ6 · rs2835872
See detailed info → StandardTRPS1 · rs2737229
See detailed info →Showing 20 of 7431 · page 261 of 372
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.