12,438 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.
near PRSS36 · rs112766425
See detailed info → StandardMED4 · rs2104480
See detailed info → SensitiveDPYD · rs67376798
See detailed info → SensitiveDPYD · rs75017182
See detailed info → SensitiveDPYD · rs3918290
See detailed info → SensitiveCYP2C19 · rs4244285
See detailed info → SensitiveCYP2C19 · rs4986893
See detailed info → StandardCYP2C19 · rs12248560
See detailed info → SensitiveTPMT · rs1142345
See detailed info → SensitiveNUDT15 · rs116855232
See detailed info → Standard on its ownFCER1A · rs2251746
See detailed info → StandardPRKD2 · rs11083846
See detailed info → StandardAPOC3 · rs12286037
See detailed info → Standard3.8-1 · rs3749946
See detailed info → SensitiveINS · rs17885785
See detailed info → StandardIL23R · rs76418789
See detailed info → StandardHLA · rs117506082
See detailed info → StandardSLC6A7 · rs17656349
See detailed info → StandardTOM1 · rs138788
See detailed info → StandardINPP5E · rs10781499
See detailed info →Showing 20 of 12438 · page 602 of 622
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.