239 positions on this site are linked to Colorectal Cancer, out of 108,452 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.
CTNNB1 · rs35470271
See detailed info → Sensitivenear SLC39A11 · rs983318
See detailed info → Sensitivenear BOC · rs12635946
See detailed info → SensitiveNRXN1 · rs4971775
See detailed info → SensitiveSTK10 · rs9313579
See detailed info → SensitiveGREM1 · rs2293582
See detailed info → Sensitivenear KLF2 · rs34797592
See detailed info → SensitiveCYP17A1 · rs4919687
See detailed info → SensitiveFMN1 · rs17816465
See detailed info → SensitiveNXN · rs73975586
See detailed info → Sensitivenear STARD13 · rs9537521
See detailed info → SensitiveBABAM1 · rs4808075
See detailed info → SensitiveHHIP · rs75686861
See detailed info → SensitiveSMAD7 · rs4939567
See detailed info → SensitiveHHIP · rs11727676
See detailed info → SensitiveCDH1 · rs9924886
See detailed info → SensitiveSMAD3 · rs56324967
See detailed info → SensitiveBRCA2 · rs11571833
See detailed info → SensitiveRAD51B · rs11844632
See detailed info → SensitivePNKD · rs3731861
See detailed info →Showing 20 of 239 · page 10 of 12
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.