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.
FAM155E · rs11796357
See detailed info → SensitiveIL20RB · rs9826828
See detailed info → Standard on its ownnear CD34 · rs1318653
See detailed info → Standard on its ownIFI44L · rs273259
See detailed info → Standard on its ownSCN2A · rs3769955
See detailed info → Standard on its ownnear ATP2B1 · rs11105468
See detailed info → Standard on its ownCD46 · rs2724384
See detailed info → Standard on its ownSCN1A · rs13004083
See detailed info → StandardDEC1 · rs10817758
See detailed info → Standardnear ADO · rs58600253
See detailed info → Standard on its ownDDAH1 · rs2268667
See detailed info → StandardRAB32 · rs13220141
See detailed info → StandardSIGLEC5 · rs10414149
See detailed info → StandardNTRK2 · rs12340987
See detailed info → SensitiveSRRM1P1 · rs12682344
See detailed info → Standard on its ownPYROXD2 · rs17455577
See detailed info → Standard on its ownPYROXD2 · rs4539242
See detailed info → Standard on its ownDCST2 · rs905938
See detailed info → StandardGFRA3 · rs10040989
See detailed info → StandardATP1B1 · rs545833
See detailed info →Showing 20 of 8787 · page 322 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.