9,493 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.
ELP4 · rs555091
See detailed info → StandardCDKN2BAS · rs523096
See detailed info → Standard on its ownETFDH · rs8396
See detailed info → StandardIL29 · rs8099917
See detailed info → Standard on its ownICAM1 · rs1799969
See detailed info → SensitiveKITLG · rs995030
See detailed info → Standard on its ownFLJ44385 · rs17000918
See detailed info → StandardMC4R · rs17700144
See detailed info → StandardADCY9 · rs2531995
See detailed info → StandardTNNI3K · rs1514174
See detailed info → StandardLOC144233 · rs10875976
See detailed info → StandardCADM2 · rs13078807
See detailed info → StandardGPRC5B · rs12446554
See detailed info → StandardFTO · rs1558902
See detailed info → StandardRPTOR · rs7503807
See detailed info → StandardNEGR1 · rs3101336
See detailed info → StandardTNNI3K · rs1514177
See detailed info → StandardMC4R · rs538656
See detailed info → StandardFTO · rs1421085
See detailed info → StandardLINGO2 · rs1412239
See detailed info →Showing 20 of 9493 · page 459 of 475
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.