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.
RTEL1-TNFRSF6B · rs3787089
See detailed info → SensitiveSMAD9 · rs12427600
See detailed info → SensitiveFMN1 · rs17816465
See detailed info → SensitiveTTC22 · rs12143541
See detailed info → Sensitivenear PLEKHG6 · rs10849438
See detailed info → SensitiveHHIP · rs75686861
See detailed info → Sensitivenear SCG5 · rs16969681
See detailed info → SensitiveSLC6A18 · rs77776598
See detailed info → Sensitivenear DACT1 · rs17094983
See detailed info → SensitivePOLD3 · rs3824999
See detailed info → SensitiveLAMC1 · rs10911251
See detailed info → SensitiveGPATCH1 · rs7252505
See detailed info → Sensitivenear DUSP10 · rs6691195
See detailed info → Sensitivenear CCND2 · rs4572213
See detailed info → SensitiveSMAD7 · rs4939567
See detailed info → SensitiveCOLCA1 · rs6589219
See detailed info → SensitiveRPS21 · rs6061231
See detailed info → SensitiveCYP17A1 · rs4919687
See detailed info → SensitiveEIF3H · rs2450115
See detailed info → Sensitivenear PDGFD · rs148883465
See detailed info →Showing 20 of 8107 · page 348 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.