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.
SMC2 · rs7859034
See detailed info → SensitiveZBTB7B · rs1870940
See detailed info → SensitiveLINC01248 · rs2882274
See detailed info → SensitiveDEF8 · rs117204628
See detailed info → SensitiveU3 · rs7833199
See detailed info → SensitiveMYCN · rs57244888
See detailed info → SensitiveRGS22 · rs28884287
See detailed info → SensitiveCTSS · rs41271951
See detailed info → SensitiveFAM49A · rs340797
See detailed info → SensitiveCELF2 · rs35202367
See detailed info → SensitiveSBNO2 · rs11669443
See detailed info → SensitiveHLA-C · rs17197839
See detailed info → SensitiveLPP · rs11719821
See detailed info → SensitiveCCR12P · rs1927729
See detailed info → SensitiveBNC2 · rs10962474
See detailed info → SensitiveLPP · rs2049218
See detailed info → SensitiveALS2CR12 · rs6714430
See detailed info → SensitiveSCAF1 · rs7508601
See detailed info → SensitiveLOC101928272 · rs17486892
See detailed info → SensitiveLOC105755953 · rs74623270
See detailed info →Showing 20 of 146 · page 6 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.