7,216 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.
PITX2 · rs10033464
See detailed info → Standard on its ownPMAIP · rs8093763
See detailed info → StandardFTO · rs9930506
See detailed info → StandardIL17REL · rs5771069
See detailed info → SensitiveTNFRSF6B · rs2315008
See detailed info → SensitiveMEIS1 · rs2300478
See detailed info → StandardMTHFR · rs1801131
See detailed info → StandardGC · rs2282679
See detailed info → StandardIRF4 · rs12203592
See detailed info → StandardAPOA5 · rs662799
See detailed info → Standard on its ownEDAR · rs3827760
See detailed info → SensitiveHFE · rs1799945
See detailed info → StandardPLAG1 · rs13273123
See detailed info → StandardAPOA5 · rs12272004
See detailed info → StandardHMGA1 · rs6918981
See detailed info → SensitiveVKORC1 · rs9923231
See detailed info → SensitiveHFE · rs1800562
See detailed info → StandardAR · rs6152
See detailed info → StandardABO · rs8176719
See detailed info → StandardDARC / ACKR1 · rs2814778
See detailed info →Showing 20 of 7216 · page 360 of 361
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.