107 positions on this site are linked to Crohn's Disease, out of 103,022 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.
SLC43A3 · rs11229030
See detailed info → Sensitivenear IRF1 · rs2188962
See detailed info → SensitiveTBC1D1 · rs1487630
See detailed info → SensitiveSBNO2 · rs2024092
See detailed info → SensitiveSLCO6A1 · rs7705924
See detailed info → SensitiveIRGM · rs7714584
See detailed info → SensitiveFUT2 · rs281379
See detailed info → SensitiveTNFSF11 · rs2062305
See detailed info → SensitiveIL12RL2 · rs2058660
See detailed info → Sensitivenear TRIB1 · rs1551398
See detailed info → SensitiveIL3 · rs12521868
See detailed info → SensitiveFUT2 · rs504963
See detailed info → Sensitivenear SOX4 · rs12663356
See detailed info → SensitiveTXK · rs6837335
See detailed info → SensitivePRDM1 · rs6568421
See detailed info → SensitiveTNFSF8 · rs3810936
See detailed info → SensitiveIL12B · rs6556412
See detailed info → SensitiveTNFSF15 · rs6478109
See detailed info → SensitiveSKAP2 · rs10486483
See detailed info → SensitiveADAM30 · rs2641348
See detailed info →Showing 20 of 107 · page 5 of 6
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.