8,787 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.
GMDS · rs9378671
See detailed info → Standard on its ownOR4A47 · rs11039798
See detailed info → Standard on its ownLRP4 · rs78744550
See detailed info → Standard on its ownBRD3 · rs11795079
See detailed info → Standard on its ownCDH11 · rs35195
See detailed info → Standard on its ownCOL8A2 · rs274136
See detailed info → Standard on its ownKREMEN1 · rs33958791
See detailed info → Sensitive on its ownTHNSL2 · rs6709352
See detailed info → Standard on its ownADAMTS6 · rs13436243
See detailed info → Standard on its ownFMNL2 · rs12471183
See detailed info → Standard on its ownLINC00598 · rs11616662
See detailed info → Standard on its ownADAMTS8 · rs7930976
See detailed info → Standard on its ownPNPT1 · rs4672075
See detailed info → Standard on its ownTCF4 · rs72932713
See detailed info → Standard on its ownRABGAP1L · rs6425280
See detailed info → Standard on its ownRALGPS1 · rs146196583
See detailed info → Standard on its ownANTXR1 · rs6732795
See detailed info → Standard on its ownRXRA · rs3132307
See detailed info → StandardHTRA1 · rs72834448
See detailed info → StandardBCAS3 · rs79771286
See detailed info →Showing 20 of 8787 · page 18 of 440
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.