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.
CFDP1 · rs17696696
See detailed info → StandardTKTL1 · rs762516
See detailed info → Standard on its ownNFATC2 · rs6021270
See detailed info → Standard on its ownADAD1 · rs17388568
See detailed info → Standard on its ownPLCL1 · rs10497813
See detailed info → Standard on its ownDAB2 · rs7720838
See detailed info → StandardNANOS1 · rs658352
See detailed info → StandardPRKCI · rs112607182
See detailed info → StandardCEND1 · rs7117921
See detailed info → StandardMYL3 · rs6768627
See detailed info → StandardSPHKAP · rs35924503
See detailed info → StandardCWC27 · rs7731168
See detailed info → StandardNR3C2 · rs6535594
See detailed info → StandardSHROOM3 · rs7654754
See detailed info → StandardAGR3 · rs4410790
See detailed info → StandardHOTTIP · rs2023844
See detailed info → StandardWIPF3 · rs17158386
See detailed info → StandardTRIB1 · rs28601761
See detailed info → StandardATP1B1 · rs1200108
See detailed info → StandardMRPS14 · rs6669560
See detailed info →Showing 20 of 12426 · page 510 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.