8,790 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.
FER · rs77606373
See detailed info → Standard on its ownRORA · rs4775427
See detailed info → Standard on its ownNPLOC4 · rs67050149
See detailed info → Standard on its ownOR4A15 · rs76154806
See detailed info → Standard on its ownSYN3 · rs5754198
See detailed info → Standard on its ownBCAS3 · rs9911155
See detailed info → Standard on its ownLOC646813 · rs7103246
See detailed info → Standard on its ownLOC440040 · rs77828979
See detailed info → Standard on its ownETS2 · rs762387
See detailed info → Standard on its ownC4orf36 · rs35667731
See detailed info → Standard on its ownISOC1 · rs115630272
See detailed info → Standard on its ownLRP4 · rs78744550
See detailed info → Standard on its ownOR4P4 · rs11230523
See detailed info → Standard on its ownLPP · rs4420855
See detailed info → Standard on its ownTHADA · rs77059113
See detailed info → Standard on its ownKREMEN1 · rs33958791
See detailed info → Standard on its ownLINC01023 · rs77844865
See detailed info → Standard on its ownBRD3 · rs11795079
See detailed info → Standard on its ownBABAM2 · rs17006576
See detailed info → Standard on its ownBABAM2 · rs6741499
See detailed info →Showing 20 of 8790 · page 17 of 440
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.