12,469 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.
RIN3 · rs10498635
See detailed info → StandardSLC6A20 · rs17279437
See detailed info → SensitiveIGF2BP2 · rs1470579
See detailed info → SensitiveHNF1A · rs7957197
See detailed info → StandardSCYL1 · rs17146964
See detailed info → Standard on its ownELOVL2 · rs2236212
See detailed info → SensitiveESR1 · rs9383938
See detailed info → SensitiveBIN1 · rs7561528
See detailed info → SensitiveMCF2L · rs11842874
See detailed info → Standard on its ownRNPEP · rs4950806
See detailed info → StandardNT5E · rs494562
See detailed info → SensitiveKCNQ1 · rs231362
See detailed info → SensitiveGNL3 · rs11177
See detailed info → StandardCF1 · rs10033900
See detailed info → StandardSH2B3 · rs4766578
See detailed info → Standard on its ownLOC728241 · rs17007761
See detailed info → SensitiveLPL · rs268
See detailed info → SensitiveCCNE1 · rs8102137
See detailed info → StandardHERC2 · rs1129038
See detailed info → Standard on its ownUBR5 · rs7840202
See detailed info →Showing 20 of 12469 · page 575 of 624
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.