8,107 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.
near GRIA1 · rs12522290
See detailed info → Sensitivenear LUZP2 · rs12360997
See detailed info → Sensitivenear RPP21 · rs114200269
See detailed info → Sensitivenear ASPG · rs112973353
See detailed info → SensitivePEPD · rs10425465
See detailed info → SensitiveCENPM · rs1023500
See detailed info → Standard on its ownSLC17A3 · rs79920061
See detailed info → Sensitivenear POU5F1B · rs72725879
See detailed info → Sensitivenear POU5F1B · rs116041037
See detailed info → SensitiveKLF12 · rs11841589
See detailed info → SensitiveAKT1 · rs2498796
See detailed info → StandardSEMA3C · rs60839105
See detailed info → Standard on its ownPFDN4 · rs6013915
See detailed info → Standard on its ownISX · rs10483182
See detailed info → Standard on its ownFGF9 · rs12583553
See detailed info → Standard on its ownARHGAP40 · rs6027072
See detailed info → Standardnear COPZ2 · rs11656818
See detailed info → Sensitivenear NMUR2 · rs79212538
See detailed info → SensitiveSDCCAG8 · rs77149735
See detailed info → SensitiveEPC2 · rs76355118
See detailed info →Showing 20 of 8107 · page 251 of 406
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.