9,253 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.
DBH · rs3025343
See detailed info → StandardBDNF · rs6265
See detailed info → SensitiveDUSP10 · rs6687758
See detailed info → SensitiveNOD2 · rs2076756
See detailed info → SensitiveIL23R · rs11209026
See detailed info → StandardUGT2A1 / UGT2A2 · rs7688383
See detailed info → StandardOR2M7 · rs4481887
See detailed info → StandardTAAR5 · rs41286168
See detailed info → Standard on its ownRBFOX3 · rs898534
See detailed info → StandardMC1R · rs12931267
See detailed info → SensitiveDUSP9 · rs5945326
See detailed info → SensitiveCENTD2 · rs1552224
See detailed info → SensitiveFTO · rs8050136
See detailed info → StandardZNF259 · rs964184
See detailed info → SensitiveAPOE · rs2075650
See detailed info → StandardSRBD1 · rs3213787
See detailed info → Standard on its ownC4BPB · rs3813948
See detailed info → StandardPITX2 · rs10033464
See detailed info → Standard on its ownPMAIP · rs8093763
See detailed info → StandardFTO · rs9930506
See detailed info →Showing 20 of 9253 · page 461 of 463
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.