7,972 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.
TET2 · rs1391440
See detailed info → Standard on its ownENSG00000245864 · rs254781
See detailed info → Sensitivenear CCND1 · rs75915166
See detailed info → Sensitivenear TENT5A · rs17529111
See detailed info → SensitiveATXN7 · rs1053338
See detailed info → Sensitivenear TERT · rs2736108
See detailed info → Sensitivenear CCND1 · rs78540526
See detailed info → SensitiveLINC00536 · rs13267382
See detailed info → SensitiveFLJ43663 · rs4593472
See detailed info → Sensitivenear CBX8 · rs745570
See detailed info → Standard on its ownCFHR4 · rs78239784
See detailed info → Standard on its ownUBE2MP1 · rs12599106
See detailed info → Standard on its ownC16orf72 · rs9039
See detailed info → Standard on its ownDMC1 · rs763121
See detailed info → Standard on its ownEIF3M · rs10734411
See detailed info → Standard on its ownPIWIL1 · rs12824058
See detailed info → Standard on its ownBRSK1 · rs2547274
See detailed info → Standard on its ownRPAIN · rs8070740
See detailed info → Standard on its ownSTARD3 · rs2941505
See detailed info → Standard on its ownCHEK2 · rs5762534
See detailed info →Showing 20 of 7972 · page 33 of 399
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.