9,513 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.
KCNJ6 · rs2835872
See detailed info → StandardTRPS1 · rs2737229
See detailed info → SensitiveTEC · rs2664035
See detailed info → SensitiveTNFAIP3 · rs7752903
See detailed info → SensitiveHLA region · rs6935723
See detailed info → StandardPOU3F2 · rs1487441
See detailed info → StandardRNF123 · rs9858213
See detailed info → StandardPDE3B · rs11023332
See detailed info → StandardCYP2R1 · rs1007392
See detailed info → StandardASB18 · rs13401104
See detailed info → StandardLRRN2 · rs3789044
See detailed info → StandardGC · rs17467825
See detailed info → Standard on its ownMIR4723 · rs704
See detailed info → Standard on its ownCOLEC10 · rs1425053
See detailed info → Standard on its ownEIF4G3 · rs4654899
See detailed info → StandardDGKK · rs4554617
See detailed info → SensitiveTANC1 · rs7582141
See detailed info → StandardCETP · rs118146573
See detailed info → StandardSIK3 · rs11216230
See detailed info → StandardTAX1BP1 · rs10214930
See detailed info →Showing 20 of 9513 · page 366 of 476
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.