8,459 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.
NOX4 · rs957140
See detailed info → Standard on its ownSLC17A3 · rs548987
See detailed info → SensitiveMAPT · rs1981997
See detailed info → Standard on its ownNOX4 · rs7130284
See detailed info → Standard on its ownDPEP1 · rs154657
See detailed info → StandardC21orf34 · rs2823615
See detailed info → StandardCYP19A1 · rs3751599
See detailed info → Standard on its ownBHMT2 · rs17823642
See detailed info → StandardIPPK · rs9969804
See detailed info → SensitiveSLC30A7 · rs11581062
See detailed info → SensitiveVTI1A · rs7086803
See detailed info → SensitiveTP63 · rs4488809
See detailed info → SensitiveZNF767 · rs354033
See detailed info → Standard on its ownTERC · rs1317082
See detailed info → Standard on its ownCDKN2B-ASI · rs1537377
See detailed info → Standard on its ownGREB1 · rs13394619
See detailed info → Standard on its ownACADL · rs3764913
See detailed info → Standard on its ownPRSS56 · rs1656404
See detailed info → StandardNUDT19 · rs3892630
See detailed info → StandardRAD51B · rs8017304
See detailed info →Showing 20 of 8459 · page 342 of 423
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.