9,570 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.
XIRP2 · rs1967279
See detailed info → Standard on its ownMANBA · rs12509403
See detailed info → Standard on its ownVPRBP · rs62257549
See detailed info → Standard on its ownHLA-DQB1 · rs34004019
See detailed info → Standard on its ownCXCR5 · rs28361986
See detailed info → Standard on its ownPLCL1 · rs2164068
See detailed info → Standard on its ownGSDMB · rs12939457
See detailed info → Standard on its ownNFATC2 · rs3787184
See detailed info → Standard on its ownCAPSL · rs7717955
See detailed info → StandardPSORS1C1 · rs17192757
See detailed info → SensitiveARHGAP6 · rs17321482
See detailed info → StandardLSAMP · rs67932684
See detailed info → StandardSCAND3 · rs146918648
See detailed info → StandardELFN1 · rs55893771
See detailed info → Standardnear OR2J2 · rs114224598
See detailed info → StandardCDYL · rs12204701
See detailed info → StandardTRIM27 · rs41286287
See detailed info → StandardMST1 · rs7613360
See detailed info → StandardCELF4 · rs55731231
See detailed info → StandardDCC · rs17681615
See detailed info →Showing 20 of 9570 · page 5 of 479
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.