Links from this page to related variants, conditions, drugs and topics are not included for automated readers. Those connections are the Gene Knowledge Graph and are licensed as data: https://www.mygenelog.com/license
UGT1A1 · rs4148324
See detailed info → SensitiveUGT1A1 · rs1042640
See detailed info → StandardUGT1A1 · rs587784535
See detailed info → SensitiveUGT1A1 · rs1373930486
See detailed info → SensitiveUGT1A1 · rs2126038220
See detailed info → SensitiveUGT1A1 · rs587776764
See detailed info → SensitiveUGT1A1 · rs367897068
See detailed info → SensitiveUGT1A1 · rs72551349
See detailed info → SensitiveUGT1A1 · rs1476500325
See detailed info → StandardUGT1A1 · rs1424603943
See detailed info → SensitiveUGT1A1 · rs72551340
See detailed info → SensitiveUGT1A1 · rs139607673
See detailed info → SensitiveUGT1A1 · rs72551343
See detailed info → SensitiveUGT1A1 · rs72551353
See detailed info → SensitiveUGT1A1 · rs72551350
See detailed info → SensitiveUGT1A1 · rs56059937
See detailed info → SensitiveUGT1A1 · rs34993780
See detailed info → SensitiveUGT1A1 · rs62625011
See detailed info → Standardnear UGT1A11P · rs184026545
See detailed info → StandardUGT1A10 · rs138562568
See detailed info →Showing 20 of 264 · page 1 of 14
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.