8,605 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.
POU6F2 · rs4549685
See detailed info → Standard on its ownCIR1 · rs72917544
See detailed info → Standard on its ownHLA-DRB1 · rs2760975
See detailed info → StandardPRKAG2 · rs62478245
See detailed info → Standard on its ownSTAU2 · rs11774977
See detailed info → Standard on its ownnear FOXF2 · rs11756214
See detailed info → Standard on its ownnear CDYL2 · rs117538856
See detailed info → Standard on its ownnear BHLHE40 · rs11715919
See detailed info → Standard on its ownnear KLF12 · rs11619505
See detailed info → SensitiveNEGR1 · rs2422320
See detailed info → SensitiveMUC21 · rs9368649
See detailed info → SensitiveUGT1A1 · rs929596
See detailed info → SensitiveUGT1A6 · rs2070959
See detailed info → SensitiveMROH2A · rs2361502
See detailed info → Sensitivenear UGT1A8 · rs2741027
See detailed info → Standard on its ownnear TMEM18 · rs6725549
See detailed info → SensitiveUGT1A6 · rs17863787
See detailed info → Standard on its ownMFAP3 · rs815610
See detailed info → Standard on its ownGIN1 · rs115505614
See detailed info → Standard on its ownCADM2 · rs13068138
See detailed info →Showing 20 of 8605 · page 22 of 431
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.