7,939 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.
FOXP1 · rs6779258
See detailed info → Standard on its ownNCKIPSD · rs73078367
See detailed info → Standard on its ownRP11-493K19.3 · rs2526388
See detailed info → Standard on its ownRBM6 · rs35849525
See detailed info → Standard on its ownNKIRAS1 · rs11129127
See detailed info → Standard on its ownNKIRAS1 · rs2001209
See detailed info → Standard on its ownNR1D2 · rs7431278
See detailed info → Standard on its ownNR1D2 · rs7631394
See detailed info → Standard on its ownSEMA3F · rs2624839
See detailed info → Standard on its ownCAMKV · rs6446187
See detailed info → Standard on its ownERBB4 · rs4132462
See detailed info → Standard on its ownTBR1 · rs116175783
See detailed info → Standard on its ownDPP4 · rs4664446
See detailed info → Standard on its ownRNA5SP107 · rs10198948
See detailed info → Standard on its ownRBMS1 · rs62175972
See detailed info → Standard on its ownRN7SL423P · rs114952970
See detailed info → Standard on its ownENSG00000232337 · rs7586673
See detailed info → Standard on its ownRNU6-1001P · rs12993989
See detailed info → Standard on its ownRBMS1 · rs10192369
See detailed info → Standard on its ownENSG00000235724 · rs7309
See detailed info →Showing 20 of 7939 · page 34 of 397
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.