240 positions on this site are linked to Colorectal Cancer, out of 108,788 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.
SMAD9 · rs12427600
See detailed info → SensitiveCOL4A2 · rs7993934
See detailed info → SensitiveVTI1A · rs12241008
See detailed info → Sensitivenear PLCL1 · rs11893063
See detailed info → SensitiveRHPN2 · rs28840750
See detailed info → SensitiveRHPN2 · rs10411210
See detailed info → SensitiveMHC · rs116353863
See detailed info → Sensitivenear SRSF3 · rs1321310
See detailed info → SensitiveEIF3H · rs2450115
See detailed info → SensitiveAPC · rs755229494
See detailed info → Sensitivenear PDGFD · rs148883465
See detailed info → SensitiveTTC22 · rs12143541
See detailed info → Sensitivenear TBRG4 · rs12672022
See detailed info → SensitiveGREM1 · rs12708491
See detailed info → SensitiveCCND2 · rs35808169
See detailed info → SensitiveTGFB1 · rs1800469
See detailed info → SensitivePOLD3 · rs3824999
See detailed info → Sensitivenear SCG5 · rs16969681
See detailed info → SensitiveEFCAB2 · rs201395236
See detailed info → Sensitivenear TET2 · rs17035289
See detailed info →Showing 20 of 240 · page 9 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.