7,839 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.
TJP2 · rs11145488
See detailed info → StandardTOX · rs10089517
See detailed info → StandardCEP164 · rs117619191
See detailed info → StandardACACB · rs149793040
See detailed info → StandardAPOA1 · rs12718462
See detailed info → StandardSLC14A2 · rs10853531
See detailed info → StandardSKIL · rs9682041
See detailed info → Standard on its ownnear HLA-DRB1 · rs2516049
See detailed info → SensitiveMIR4686 · rs7107784
See detailed info → SensitiveATP8B2 · rs67156297
See detailed info → SensitiveASB3 · rs9309245
See detailed info → SensitiveDMRTA1 · rs1575972
See detailed info → SensitiveCCDC85A · rs1116357
See detailed info → Standard on its ownBTNL2 · rs4248166
See detailed info → SensitiveIGF2BP2 · rs4481184
See detailed info → SensitivePPARG · rs2881654
See detailed info → SensitiveFAF1 · rs3789588
See detailed info → SensitiveMTOR · rs1010447
See detailed info → SensitiveSYNJ1 · rs147991290
See detailed info → SensitiveSDR42E2 · rs145049847
See detailed info →Showing 20 of 7839 · page 229 of 392
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.