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.
NAALAD2 · rs11018904
See detailed info → Standard on its ownC12orf36 · rs1479119
See detailed info → Standard on its ownENSG00000258028 · rs1998358
See detailed info → Standard on its ownENSG00000257522 · rs17641673
See detailed info → Standard on its ownENSG00000258232 · rs11168951
See detailed info → Standard on its ownPRKD1 · rs971681
See detailed info → Standard on its ownAKAP6 · rs4261436
See detailed info → Standard on its ownNCOA2 · rs57994514
See detailed info → Standard on its ownRALYL · rs117893056
See detailed info → Standard on its ownFGF8 · rs7077446
See detailed info → Standard on its ownC10orf76 · rs67497633
See detailed info → Standard on its ownSORCS3 · rs1947988
See detailed info → Standard on its ownC10orf76 · rs117883100
See detailed info → Standard on its ownHPS6 · rs11191205
See detailed info → Standard on its ownPHF2 · rs10992797
See detailed info → Standard on its ownENSG00000201074 · rs13287066
See detailed info → Standard on its ownCDC14B · rs6477493
See detailed info → Standard on its ownJMJD1C · rs6479901
See detailed info → Standard on its ownRUNX1T1 · rs2916247
See detailed info → Standard on its ownLRRC14 · rs2721173
See detailed info →Showing 20 of 8057 · page 31 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.