9,253 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.
near RPS29 · rs57679537
See detailed info → StandardSYNE2 · rs1152595
See detailed info → StandardNOVA1 · rs178184
See detailed info → StandardAKAP5 · rs3742608
See detailed info → Standardnear NKX2-8 · rs1007731
See detailed info → StandardRGS6 · rs12897542
See detailed info → Standardnear TTC8 · rs11845781
See detailed info → Standardnear NALF1 · rs75141555
See detailed info → StandardNRL · rs11623285
See detailed info → StandardLIN52 · rs2358628
See detailed info → StandardUNC79 · rs6575340
See detailed info → StandardSYNDIG1L · rs730384
See detailed info → Standardnear LHX5 · rs3809169
See detailed info → StandardDYNLL1 · rs616157
See detailed info → StandardPOLR3B · rs11113011
See detailed info → Standardnear MLXIP · rs11058322
See detailed info → StandardTMTC4 · rs9300612
See detailed info → StandardPCCA · rs9513754
See detailed info → Standardnear PCDH17 · rs9527662
See detailed info → Standardnear PCDH17 · rs7325960
See detailed info →Showing 20 of 9253 · page 8 of 463
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.