12,426 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.
MC4R · 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 → StandardADCY3 · rs10182181
See detailed info → StandardTFAP2B · rs2206277
See detailed info → StandardGIPR · rs1800437
See detailed info → StandardC5orf37 · rs2112347
See detailed info → StandardNEGR1 · rs7531118
See detailed info → StandardGPRC5B · rs12446632
See detailed info → StandardGNPDA2 · rs10938397
See detailed info →Showing 20 of 12426 · page 606 of 622
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.