12,481 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.
HLA-DRB5 · rs674313
See detailed info → SensitiveC6orf57 · rs1048886
See detailed info → StandardZMYND8 · rs910187
See detailed info → StandardPRKCB · rs9939355
See detailed info → StandardTERF2 · rs528301822
See detailed info → StandardZNF521 · rs962247
See detailed info → StandardCELF4 · rs2861805
See detailed info → StandardPSMG1 · rs2836909
See detailed info → StandardLTBR-TNFRSF1A · rs11616188
See detailed info → StandardNRXN3 · rs2370926
See detailed info → StandardFLG · rs3126085
See detailed info → StandardNAALAD2 · rs11018874
See detailed info → StandardHBS1L · rs9373124
See detailed info → StandardHLA-DPA1 · rs3077
See detailed info → StandardSTARD13 · rs9315204
See detailed info → StandardMMP13 · rs74380195
See detailed info → StandardRPL27A · rs4929949
See detailed info → StandardIL12A · rs6441286
See detailed info → StandardDCAF12 · rs62560863
See detailed info → StandardFOCAD · rs10811438
See detailed info →Showing 20 of 12481 · page 557 of 625
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.