12,488 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.
HMGA2 · rs1042725
See detailed info → Standard on its ownRNF146 · rs4273712
See detailed info → Standard on its ownCAPZB · rs10917468
See detailed info → Standard on its ownMAF · rs17767419
See detailed info → StandardNT5C2 · rs11191593
See detailed info → StandardMAP4 · rs319690
See detailed info → Standardnear ZBTB40 · rs6684375
See detailed info → StandardCPED1 · rs13245690
See detailed info → StandardPPP6R3 · rs12284933
See detailed info → SensitiveTNIP1 · rs2233287
See detailed info → Standardnear TNFSF11 · rs9525638
See detailed info → SensitiveKRT8 · rs902774
See detailed info → StandardTNRC6B · rs12484776
See detailed info → SensitiveCD2AP · rs9349407
See detailed info → StandardMHC · rs2516399
See detailed info → Standard on its ownCAPZB · rs12045440
See detailed info → SensitiveCSF1 · rs10494112
See detailed info → SensitivePRNP · rs1799990
See detailed info → StandardTNFAIP2 · rs8017161
See detailed info → StandardIL12RB2 · rs17129789
See detailed info →Showing 20 of 12488 · page 553 of 625
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.