7,670 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.
HLA-DPB1 · rs1431403
See detailed info → SensitiveUHRF1BP1 · rs6457796
See detailed info → SensitiveBACH2 · rs3857496
See detailed info → SensitiveLRRC25 · rs13344313
See detailed info → SensitiveTRAF3 · rs12148050
See detailed info → SensitiveIPCEF1 · rs9322454
See detailed info → SensitiveLOC101926943 · rs117026326
See detailed info → Sensitivenear TRPA1 · rs10111413
See detailed info → SensitiveLINC00824 · rs16902895
See detailed info → SensitiveST8SIA4 · rs12153670
See detailed info → SensitiveNCF1 · rs73366469
See detailed info → SensitiveCD58 · rs1016140
See detailed info → SensitiveLINC00824 · rs7815944
See detailed info → SensitiveIFNA22P · rs7858766
See detailed info → SensitiveANKRD16 · rs77448389
See detailed info → SensitiveBBIP1 · rs58164562
See detailed info → SensitiveC1QTNF12 · rs12093154
See detailed info → SensitiveTNPO3 · rs78724056
See detailed info → SensitiveIRF5 · rs41298401
See detailed info → SensitiveHIP1 · rs4573208
See detailed info →Showing 20 of 7670 · page 259 of 384
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.