10,922 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.
SYN2 · rs7616006
See detailed info → StandardGNL3 · rs2590838
See detailed info → StandardEHD3 · rs625132
See detailed info → Standard on its ownAUTS2 · rs1403155
See detailed info → Standard on its ownCNTN5 · rs11223581
See detailed info → StandardARHGEF3 · rs1354034
See detailed info → StandardTHADA · rs17030845
See detailed info → StandardLPA · rs12208357
See detailed info → StandardHP · rs11648003
See detailed info → StandardFAM117B · rs115400054
See detailed info → StandardMLXIPL · rs3812316
See detailed info → StandardJAG1 · rs1327235
See detailed info → StandardLIPC · rs1601935
See detailed info → StandardAPOB · rs1041968
See detailed info → StandardLDLR · rs112374545
See detailed info → StandardHLA-area · rs114067101
See detailed info → StandardLIPG · rs149615216
See detailed info → SensitiveDUSP10 · rs6691170
See detailed info → StandardLCAT · rs2271293
See detailed info → StandardLIPC · rs10468017
See detailed info →Showing 20 of 10922 · page 495 of 547
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.