12,425 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.
PAM · rs526231
See detailed info → StandardADAM28 · rs1013209
See detailed info → StandardLYPLAL1 · rs11118346
See detailed info → StandardINSR · rs891088
See detailed info → StandardETV6 · rs2856321
See detailed info → StandardPEX2 · rs6473015
See detailed info → StandardPCCB · rs9844666
See detailed info → Standard on its ownRUNX1 · rs2242882
See detailed info → StandardBOD1 · rs889014
See detailed info → StandardHLA locus · rs6457620
See detailed info → Standard on its ownHLA-DQA2 · rs2858331
See detailed info → Standard on its ownPDGFRA · rs7677751
See detailed info → Standard on its ownOR10J3 · rs4656784
See detailed info → StandardSLC16A9 · rs7094971
See detailed info → Standard on its ownBDNF · rs75945125
See detailed info → Standard on its ownRUNX1 · rs71329093
See detailed info → Standard on its ownEGR2 · rs224278
See detailed info → SensitiveEBF1 · rs1432679
See detailed info → StandardCFHR3 · rs6677604
See detailed info → StandardVAV3 · rs17019602
See detailed info →Showing 20 of 12425 · page 517 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.