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 LINC02674 · rs7098111
See detailed info → SensitiveDCST1 · rs55668940
See detailed info → Sensitivenear HLA-DQA1 · rs9271611
See detailed info → SensitiveFLACC1 · rs7582362
See detailed info → SensitiveZNF365 · rs10995255
See detailed info → SensitiveAC010745.4 · rs6739779
See detailed info → SensitiveTHNSL2 · rs6707137
See detailed info → SensitiveFAM157C · rs56407236
See detailed info → SensitiveCUX1 · rs78227582
See detailed info → SensitiveLINC01111 · rs10216564
See detailed info → SensitiveSPIRE2 · rs45609834
See detailed info → SensitiveCFL1 · rs10896064
See detailed info → SensitiveBCAS4 · rs62202837
See detailed info → SensitiveMYO15A · rs854807
See detailed info → SensitiveZFHX4 · rs28727938
See detailed info → SensitiveRP4-799G3.2 · rs12070203
See detailed info → SensitiveRP11-428L9.1 · rs138501911
See detailed info → SensitiveLOC100506274 · rs79522206
See detailed info → SensitiveCTSH · rs2289702
See detailed info → SensitivePPARGC1B · rs109077
See detailed info →Showing 20 of 146 · page 5 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.