8,812 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.
BACH2 · rs1847472
See detailed info → SensitivePHACTR2 · rs12199775
See detailed info → SensitiveYDJC · rs2266959
See detailed info → Standard on its ownMYO1D · rs17183295
See detailed info → Standard on its ownTJP2 · rs11145465
See detailed info → Standard on its ownCYP26A1 · rs10882165
See detailed info → StandardAIFM3 · rs756878
See detailed info → SensitiveESR1 · rs140068132
See detailed info → Standard on its ownHORMAD2 · rs2412971
See detailed info → StandardHOXB1 · rs12948086
See detailed info → StandardAAGAB · rs12912010
See detailed info → StandardKLF5 · rs17285550
See detailed info → StandardRORA · rs76194223
See detailed info → StandardAP4E1 · rs11634895
See detailed info → SensitiveAPOE · rs429358
See detailed info → Standard on its ownPHB2 · rs2110073
See detailed info → Standard on its ownMBOAT5 · rs12580543
See detailed info → Standard on its ownEXOG · rs7433306
See detailed info → Standard on its ownPRDM16 · rs2483280
See detailed info → Standard on its ownHLA · rs12195582
See detailed info →Showing 20 of 8812 · page 326 of 441
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.