8,083 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.
ELAVL2 · rs10119773
See detailed info → Standardnear FAM120AOS · rs55766809
See detailed info → Standard on its ownARL17B · rs2696532
See detailed info → Standard on its ownATAD2B · rs7569424
See detailed info → Standard on its ownCNTNAP5 · rs780024
See detailed info → Standard on its ownUBXN2A · rs12616250
See detailed info → Standardnear PTCH1 · rs112191650
See detailed info → Standard on its ownnear GRIK3 · rs681875
See detailed info → Standard on its ownKLHL29 · rs34657012
See detailed info → StandardMADD · rs11039182
See detailed info → Standard on its ownMICA · rs4360170
See detailed info → Standard on its ownCA10 · rs1392935
See detailed info → Standard on its ownGGNBP2 · rs3744593
See detailed info → Standard on its ownTMPRSS5 · rs7939917
See detailed info → Standard on its ownIST1 · rs4788570
See detailed info → Standard on its ownNUPR1 · rs12446550
See detailed info → Standard on its ownDENND4A · rs72741274
See detailed info → Standard on its ownCCDC101 · rs480400
See detailed info → Standard on its ownIVD · rs2289328
See detailed info → Standard on its ownDLL4 · rs12441495
See detailed info →Showing 20 of 8083 · page 30 of 405
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.