7,839 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.
INSR · rs891088
See detailed info → Standard on its ownPDGFRA · rs7677751
See detailed info → StandardBOD1 · rs889014
See detailed info → Standard on its ownEGR2 · rs224278
See detailed info → Standard on its ownRUNX1 · rs2242882
See detailed info → Standard on its ownOR10J3 · rs4656784
See detailed info → Standard on its ownBDNF · rs75945125
See detailed info → Standard on its ownRUNX1 · rs71329093
See detailed info → StandardHLA locus · rs6457620
See detailed info → Standard on its ownHLA-DQA2 · rs2858331
See detailed info → Standard on its ownSLC16A9 · rs7094971
See detailed info → Standard on its ownCFHR3 · rs6677604
See detailed info → Standard on its ownNPPB · rs198389
See detailed info → SensitiveEBF1 · rs1432679
See detailed info → Standard on its ownVAV3 · rs17019602
See detailed info → SensitiveNOSIP · rs56873913
See detailed info → SensitiveZNF536 · rs2053079
See detailed info → SensitiveCILP2 · rs2905426
See detailed info → SensitiveSGSM2 · rs4523957
See detailed info → SensitiveACD · rs8044995
See detailed info →Showing 20 of 7839 · page 288 of 392
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.