10,689 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.
PTPN9 · rs12904319
See detailed info → Standard on its ownAC016735.1 · rs115262049
See detailed info → Standard on its own7SK · rs62039768
See detailed info → Standard on its ownTFAP2B · rs3857599
See detailed info → Standard on its ownRP11-344J7.2 · rs9472136
See detailed info → Standard on its ownPTP4A3 · rs12549801
See detailed info → Standard on its ownUSP24 · rs530804537
See detailed info → Standard on its ownRP4-662A9.2 · rs2105092
See detailed info → Standard on its ownAP001046.5 · rs762395
See detailed info → StandardZNF318 · rs7742789
See detailed info → Standard on its ownTBC1D19 · rs28667801
See detailed info → Standard on its ownCDC25A · rs6800730
See detailed info → Standard on its ownCNTF · rs11229555
See detailed info → Standard on its ownPPAP2B · rs61772578
See detailed info → Standard on its ownHDAC4 · rs62182100
See detailed info → Standard on its ownEFCAB4B · rs242016
See detailed info → Standard on its ownnear ETAA1 · rs56225803
See detailed info → Standard on its ownnear GPR132 · rs56256371
See detailed info → Standard on its ownTGM6 · rs6114027
See detailed info → StandardPNPT1 · rs706550
See detailed info →Showing 20 of 10689 · page 4 of 535
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.