146 positions on this site are linked to Basal Cell Carcinoma, out of 118,864 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.
near IRF4 · rs2797304
See detailed info → Sensitivenear GAPDHP77 · rs12833418
See detailed info → SensitiveCHMP1A · rs71396949
See detailed info → SensitiveCFL1 · rs548082010
See detailed info → Sensitivenear GACAT3 · rs73215860
See detailed info → Sensitivenear MRPL45P1 · rs6547771
See detailed info → Sensitivenear LINC02929 · rs12766391
See detailed info → SensitiveLINC02676 · rs11255972
See detailed info → Sensitivenear RNU6ATAC37P · rs76629241
See detailed info → SensitiveBNC2 · rs10962600
See detailed info → Sensitivenear KRT6A · rs599466
See detailed info → SensitiveDEF8 · rs7195043
See detailed info → SensitiveHLA-DRB9 · rs9268847
See detailed info → SensitiveFOXP1 · rs6764416
See detailed info → SensitiveSCAF1 · rs2082481
See detailed info → Sensitivenear SMC2 · rs10820610
See detailed info → Sensitivenear BNC2 · rs369593216
See detailed info → SensitiveRGS22 · rs28410444
See detailed info → SensitiveLINC02676 · rs76407406
See detailed info → Sensitivenear Y_RNA · rs7818943
See detailed info →Showing 20 of 146 · page 2 of 8
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.