9,215 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.
HACE1 · rs1475120
See detailed info → SensitiveSORCS3 · rs10786831
See detailed info → SensitivePAX5 · rs6476606
See detailed info → SensitiveRSRC1 · rs1656369
See detailed info → SensitiveNEGR1 · rs2422321
See detailed info → Standard on its ownTCF4 · rs144933108
See detailed info → Standard on its ownnear TCF4 · rs72932578
See detailed info → Standard on its ownTCF4 · rs188837888
See detailed info → Standard on its ownANAPC1 · rs200632716
See detailed info → Standard on its ownCALN1 · rs35526560
See detailed info → Standard on its ownAUTS2 · rs12112638
See detailed info → Standard on its ownnear BLID · rs76561503
See detailed info → StandardAP000721.4 · rs4980515
See detailed info → StandardWDR7 · rs10048404
See detailed info → StandardCTD-2260A17.2 · rs709668
See detailed info → StandardATP2B1 · rs10858966
See detailed info → StandardPDGFC · rs17035181
See detailed info → StandardMARK3 · rs8014182
See detailed info → StandardWHSC1L1 · rs1906672
See detailed info → StandardTOP3A · rs4925159
See detailed info →Showing 20 of 9215 · page 9 of 461
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.