102,980 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 OPRM1 · rs1772945
See detailed info → StandardOPRM1 · rs1294093
See detailed info → StandardOPRM1 · rs13193545
See detailed info → SensitiveOPRM1 · rs3778151
See detailed info → StandardOPRM1 · rs514980
See detailed info → StandardOPRM1 · rs9688977
See detailed info → StandardOPRM1 · rs79910351
See detailed info → StandardOPRM1 · rs3778150
See detailed info → StandardOPRM1 · rs696523
See detailed info → StandardOPRM1 · rs7773995
See detailed info → StandardOPRM1 · rs17181171
See detailed info → StandardOPRM1 · rs73568641
See detailed info → Standardnear OPRM1 · rs10499276
See detailed info → StandardOPRM1 · rs1799971
See detailed info →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.