9,043 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.
SLC4A7 · rs4973768
See detailed info → Standard on its ownG6PC2 · rs560887
See detailed info → SensitiveBMP4 · rs4444235
See detailed info → SensitiveKCNQ1 · rs2237897
See detailed info → Standard on its ownCAV1 · rs3807989
See detailed info → SensitiveKIAA0350 · rs12708716
See detailed info → StandardTRIB1 · rs2954029
See detailed info → StandardLPL · rs12678919
See detailed info → SensitiveMAP2K5 · rs12593813
See detailed info → StandardGALNT2 · rs4846914
See detailed info → SensitiveEHBP1 · rs721048
See detailed info → SensitiveADAMTS7 · rs1994016
See detailed info → SensitiveKCNQ1 · rs2237892
See detailed info → StandardCETP · rs3764261
See detailed info → Standard on its ownZBTB40 · rs7524102
See detailed info → Standard on its ownLY75 · rs4664308
See detailed info → Standard on its ownRBBP8 · rs11661542
See detailed info → SensitiveC12orf30 · rs17696736
See detailed info → StandardATP2B1 · rs17249754
See detailed info → StandardAPIP · rs12793173
See detailed info →Showing 20 of 9043 · page 449 of 453
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.