12,444 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.
ATP2B1 · rs2681472
See detailed info → SensitiveDQ141194 · rs7741164
See detailed info → Standard on its ownEPGN · rs16850885
See detailed info → StandardGSTCD · rs11727189
See detailed info → StandardAGER · rs2070600
See detailed info → Sensitivenear SMIM38 · rs11228565
See detailed info → SensitiveSPINT2 · rs8102476
See detailed info → StandardLOC646909 · rs10091038
See detailed info → StandardGMDS · rs6914444
See detailed info → StandardCADM2 · rs9284802
See detailed info → StandardEXOC2 · rs57111852
See detailed info → StandardLOC154449 · rs2935072
See detailed info → StandardCAV1 · rs2024211
See detailed info → StandardUBASH3A · rs11203203
See detailed info → StandardSALL1 · rs1362756
See detailed info → StandardRNASET2 · rs2236313
See detailed info → SensitiveCD58 · rs2300747
See detailed info → StandardRNF11 · rs17391905
See detailed info → StandardTPMT · rs10949482
See detailed info → SensitiveBNC2 · rs3814113
See detailed info →Showing 20 of 12444 · page 600 of 623
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.