12,512 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.
IRF5 · rs3757387
See detailed info → SensitiveSMG7 · rs17849501
See detailed info → StandardTOMM40 · rs1160985
See detailed info → StandardLEPR · rs1805096
See detailed info → Standard on its ownSSTR1 · rs11622412
See detailed info → SensitiveIRF5 · rs729302
See detailed info → StandardEXO1 · rs1635501
See detailed info → SensitiveCDKN1B · rs34330
See detailed info → SensitiveCD80 · rs6804441
See detailed info → SensitiveDGUOK · rs4852324
See detailed info → SensitiveDGUOK · rs6705628
See detailed info → Standardnear ARL14EP · rs12294104
See detailed info → StandardSYCP2L · rs2153157
See detailed info → StandardTLK1 · rs10183486
See detailed info → StandardIL23R · rs3762318
See detailed info → Standard on its ownDARC · rs12075
See detailed info → SensitiveDPCR · rs114090659
See detailed info → StandardRNF7 · rs16851720
See detailed info → SensitiveSLC15A4 · rs11059919
See detailed info → SensitiveJAZF1 · rs12531540
See detailed info →Showing 20 of 12512 · page 550 of 626
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.