7,670 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.
TET2 · rs9790517
See detailed info → SensitiveMETAP1D · rs2016394
See detailed info → Standard on its ownCHSY1 · rs752092
See detailed info → Standard on its ownTJP1 · rs785422
See detailed info → Standard on its ownFOXO1 · rs2721051
See detailed info → Standard on its ownGLT8D2 · rs1564892
See detailed info → Standard on its ownARHGAP20 · rs4938174
See detailed info → Standard on its ownLCN12 · rs11145951
See detailed info → Standard on its ownCOL5A1 · rs1536482
See detailed info → Standard on its ownLPAR1 · rs1007000
See detailed info → Standard on its ownADAMTS6 · rs2307121
See detailed info → Standard on its ownFURIN · rs6227
See detailed info → Standard on its ownDARC · rs13962
See detailed info → StandardKCNH5 · rs76513344
See detailed info → Standard7SK · rs60283548
See detailed info → StandardCERS3 · rs80332023
See detailed info → StandardCYP17A1 · rs4409766
See detailed info → StandardGUCY1A3 · rs13143871
See detailed info → StandardFGF5 · rs1902859
See detailed info → StandardCYP21A2 · rs2021783
See detailed info →Showing 20 of 7670 · page 284 of 384
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.