12,477 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.
NXN · rs73975588
See detailed info → Sensitivenear TET2 · rs17035289
See detailed info → SensitiveSMAD6 · rs4776316
See detailed info → SensitiveCOL4A2 · rs7993934
See detailed info → Sensitivenear BOC · rs12635946
See detailed info → Sensitivenear SATB2 · rs7593422
See detailed info → SensitiveMAMSTR · rs12979278
See detailed info → Sensitivenear PLCL1 · rs11893063
See detailed info → SensitiveFHL3 · rs61776719
See detailed info → Sensitivenear BMP2 · rs6085661
See detailed info → SensitiveRTEL1-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 →Showing 20 of 12477 · page 566 of 624
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.