8,057 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.
PRKAG2 · rs7805747
See detailed info → SensitiveSETDB1 · rs267734
See detailed info → Standard on its ownCENPW · rs139878170
See detailed info → Standard on its ownCCND1 · rs9344
See detailed info → Standard on its ownSMARCD3 · rs79419269
See detailed info → Standard on its ownPRTN3 · rs62132293
See detailed info → Standard on its ownSPRY2 · rs693839
See detailed info → Standard on its ownTUFM · rs4788099
See detailed info → Standard on its ownCOBLL1 · rs6738627
See detailed info → Standard on its ownACCN1 · rs11652874
See detailed info → Standard on its ownIL6R · rs12133641
See detailed info → StandardNCAN · rs2238675
See detailed info → StandardKANK2 · rs138534124
See detailed info → Standard on its ownLINC00540 · rs9316871
See detailed info → StandardLINC01192 · rs62295801
See detailed info → StandardCD180 · rs9291879
See detailed info → StandardRP11-422J15.1 · rs17421787
See detailed info → StandardSLC2A9 · rs7656342
See detailed info → StandardLINC00973 · rs9831278
See detailed info → StandardSIPA1L3 · rs148330122
See detailed info →Showing 20 of 8057 · page 253 of 403
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.