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.
LMX1B · rs3829849
See detailed info → Standard on its ownADAM23 · rs13387838
See detailed info → Standard on its ownELP3 · rs13253111
See detailed info → Standard on its ownGNAT2 · rs17024393
See detailed info → Standard on its ownRAB27B · rs8092503
See detailed info → SensitivePRKAA1 · rs13361707
See detailed info → Standard on its ownEFHC1 · rs9357733
See detailed info → Standard on its ownGPR61 · rs7550711
See detailed info → Standard on its ownIL4 · rs17690965
See detailed info → Standard on its ownTNNI3K · rs12041852
See detailed info → Standard on its ownMIPOL1 · rs17106852
See detailed info → Standard on its ownnear RNASE3 · rs8007643
See detailed info → Standard on its ownnear PAX1 · rs2424399
See detailed info → SensitiveMAD1L1 · rs4332037
See detailed info → Standard on its ownHLA-DQA1 · rs35242582
See detailed info → StandardCPZ · rs2241069
See detailed info → SensitiveCXCL12 · rs1870634
See detailed info → Sensitive9p21 · rs2891168
See detailed info → SensitiveAPOC1 · rs56131196
See detailed info → SensitiveGUCY1A3 · rs72689147
See detailed info →Showing 20 of 9513 · page 283 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.