8,154 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.
IGF2R · rs688359
See detailed info → SensitiveLPL · rs264
See detailed info → SensitiveBMP1 · rs6984210
See detailed info → Sensitivenear MTAP · rs896655
See detailed info → SensitiveSVEP1 · rs111245230
See detailed info → SensitiveLPAL2 · rs147555597
See detailed info → SensitiveASZ1 · rs10249651
See detailed info → SensitiveCDKN2B · rs3217978
See detailed info → Standard on its ownWBP1L · rs284844
See detailed info → Standard on its ownSLC24A3 · rs11696394
See detailed info → Standard on its ownDOT1L · rs55678414
See detailed info → Standard on its ownnear SLC4A7 · rs12498098
See detailed info → Standard on its ownKCNK3 · rs1275978
See detailed info → SensitiveMACF1 · rs16826069
See detailed info → SensitivePAM · rs35658696
See detailed info → SensitiveKLHDC5 · rs1127787
See detailed info → Standard on its ownTYK2 · rs35164067
See detailed info → Standard on its ownDUSP10 · rs12126292
See detailed info → Standard on its ownTET2 · rs1391439
See detailed info → Standard on its ownBACH2 · rs17765610
See detailed info →Showing 20 of 8154 · page 28 of 408
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.