8,698 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.
UHRF1BP1 · rs9469899
See detailed info → Standard on its ownART4 · rs2287226
See detailed info → Standard on its ownCELF1 · rs11039266
See detailed info → Standard on its ownMLLT10 · rs1243182
See detailed info → Standard on its ownSH2B1 · rs62037364
See detailed info → Standard on its ownTMEM18 · rs35142762
See detailed info → Standard on its ownTRPS1 · rs62512210
See detailed info → Standard on its ownDNER · rs7571826
See detailed info → Standard on its ownWWP2 · rs11645565
See detailed info → Standard on its ownFAM150B · rs62107261
See detailed info → Standard on its ownRAB11FIP5 · rs58649746
See detailed info → SensitiveCPEB4 · rs72810983
See detailed info → Sensitivenear TTC33 · rs1505992
See detailed info → SensitiveIL18RAP · rs6708413
See detailed info → SensitiveCNTN4 · rs17022006
See detailed info → Standard on its ownnear GJD2 · rs670352
See detailed info → Standard on its ownDKK2 · rs17037148
See detailed info → Standard on its ownnear BCL11A · rs17025388
See detailed info → Standard on its ownnear PRR9 · rs16835093
See detailed info → Standard on its ownWARS2 · rs17023135
See detailed info →Showing 20 of 8698 · page 21 of 435
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.