10,922 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.
NOV · rs2071518
See detailed info → StandardADAMTS-8 · rs11222084
See detailed info → Standard on its ownPCSK1 · rs6235
See detailed info → Standard on its ownLARP6 · rs1549318
See detailed info → SensitiveANP32A · rs8030672
See detailed info → SensitivePLCE1 · rs2274223
See detailed info → StandardITPA · rs6139030
See detailed info → Standard on its ownSLC30A8 · rs11558471
See detailed info → StandardDOCK7 · rs2131925
See detailed info → StandardEDN3 · rs6015450
See detailed info → StandardNT5C2 · rs11191548
See detailed info → SensitiveNRG1 · rs2439302
See detailed info → SensitiveMBIP · rs116909374
See detailed info → StandardNAT8 · rs9309473
See detailed info → StandardEDNRA · rs6842241
See detailed info → StandardRAB32 · rs2275606
See detailed info → StandardCYLD · rs16948876
See detailed info → Standard on its ownFTH1 · rs174550
See detailed info → StandardTRIM58 · rs3811444
See detailed info → StandardIL5RA · rs9815663
See detailed info →Showing 20 of 10922 · page 494 of 547
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.