8,154 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.
ETV7 · rs3778028
See detailed info → StandardCLIC1 · rs145269503
See detailed info → StandardEFHC1 · rs56032325
See detailed info → Standardnear CD2AP · rs9473147
See detailed info → Standard on its ownBHMT · rs617219
See detailed info → Sensitivenear HLA-DRA · rs187696124
See detailed info → Sensitivenear SMIM38 · rs10896449
See detailed info → StandardCCDC27 · rs1181870
See detailed info → StandardADCY8 · rs17311976
See detailed info → StandardFAT1 · rs148750727
See detailed info → StandardAPH1A · rs10157197
See detailed info → StandardAK5 · rs76681500
See detailed info → StandardLINC01128 · rs141175086
See detailed info → StandardFCGR2B · rs61804164
See detailed info → StandardDNM3 · rs554019
See detailed info → StandardGDF5 · rs6060373
See detailed info → SensitiveLTBP1 · rs4630744
See detailed info → SensitiveTGFA · rs3821262
See detailed info → SensitiveSLBP · rs11732213
See detailed info → SensitiveHLA-DPB1 · rs9277552
See detailed info →Showing 20 of 8154 · page 250 of 408
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.