12,469 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.
ABO · rs507666
See detailed info → Sensitive on its ownnear OBI1 · rs11838918
See detailed info → StandardHLA-C · rs9368677
See detailed info → StandardELOVL2 · rs9393903
See detailed info → StandardSLC16A10 · rs7760535
See detailed info → StandardWNT4 · rs3765350
See detailed info → StandardCAPN3 · rs2412710
See detailed info → StandardLRP1 · rs11613352
See detailed info → StandardMAP3K1 · rs9686661
See detailed info → StandardFRMD5 · rs2929282
See detailed info → StandardCPED1 · rs2110281
See detailed info → Standardnear GALNT3 · rs6726821
See detailed info → StandardAPOC2 · rs439401
See detailed info → StandardAPOB · rs1042034
See detailed info → SensitiveFOS · rs4899554
See detailed info → StandardCPS1 · rs2216405
See detailed info → Sensitivenear ZBTB40 · rs12568930
See detailed info → SensitiveADCY3 · rs6545800
See detailed info → Sensitivenear CTH · rs2651244
See detailed info → StandardSLCO1B1 · rs4149081
See detailed info →Showing 20 of 12469 · page 578 of 624
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.