12,444 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.
IL12B · rs6556412
See detailed info → SensitiveIL12RL2 · rs2058660
See detailed info → SensitiveIL2RA · rs12722489
See detailed info → SensitiveIRGM · rs7714584
See detailed info → SensitiveHLA-DQA2 · rs1799964
See detailed info → SensitiveMAP3K7IP1 · rs2413583
See detailed info → SensitiveMUC19 · rs11564258
See detailed info → SensitivePRDM1 · rs6568421
See detailed info → SensitiveIL3 · rs12521868
See detailed info → SensitiveSP140 · rs7423615
See detailed info → SensitiveTHADA · rs10495903
See detailed info → SensitiveTNFSF11 · rs2062305
See detailed info → SensitiveTNFSF8 · rs3810936
See detailed info → SensitiveZFP36L1 · rs4902642
See detailed info → SensitiveFUT2 · rs504963
See detailed info → Sensitivenear TTC33 · rs17234657
See detailed info → SensitiveNOD2 · rs17221417
See detailed info → SensitivePTPN2 · rs2542151
See detailed info → SensitiveIRGM · rs11747270
See detailed info → Sensitivenear IRF1 · rs2188962
See detailed info →Showing 20 of 12444 · page 598 of 623
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.