7,939 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.
KCNV2 · rs10738760
See detailed info → SensitiveKIR2DL1 · rs11672983
See detailed info → SensitiveCD40 · rs1569723
See detailed info → SensitiveCEBPB · rs913678
See detailed info → SensitiveRPS6KB1 · rs1292053
See detailed info → Standard on its ownnear PPT2 · rs204999
See detailed info → SensitiveRABEP2 · rs26528
See detailed info → SensitiveCRTC3 · rs7495132
See detailed info → Standard on its ownFTO · rs12149832
See detailed info → StandardPCSK1 · rs261967
See detailed info → StandardCDKAL1 · rs9356744
See detailed info → SensitiveSCARB2 · rs6812193
See detailed info → SensitiveEXOC2 · rs12210050
See detailed info → Sensitive on its ownF11 · rs2289252
See detailed info → Sensitive on its ownSELP · rs6028
See detailed info → Standard on its ownTRIB1 · rs2980879
See detailed info → Standard on its ownTARDBP · rs12565727
See detailed info → SensitiveSLC30A8 · rs3802177
See detailed info → Standard on its ownDNAH10 · rs6488898
See detailed info → Standard on its ownADIPOQ · rs182052
See detailed info →Showing 20 of 7939 · page 353 of 397
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.