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 RHOU · rs11586259
See detailed info → Sensitivenear LINC03086 · rs874501
See detailed info → Sensitivenear Y_RNA · rs10102592
See detailed info → Sensitivenear EXOC2 · rs11961808
See detailed info → Sensitivenear LINC00111 · rs2849695
See detailed info → Sensitivenear HLA-DQA1 · rs502803
See detailed info → SensitiveRGS22 · rs6989943
See detailed info → Sensitivenear NOX4 · rs10830255
See detailed info → SensitiveRAI1 · rs9910411
See detailed info → SensitiveUBAC2 · rs7139522
See detailed info → SensitiveGABBR1 · rs29243
See detailed info → SensitiveRBM6 · rs11130229
See detailed info → SensitiveSMAD3 · rs7359174
See detailed info → SensitiveG3BP1 · rs2964574
See detailed info → Sensitivenear TLR3 · rs13120159
See detailed info → SensitiveLINC01331 · rs1001114
See detailed info → Sensitivenear LINC01248 · rs13409347
See detailed info → SensitiveST3GAL6 · rs4638909
See detailed info → SensitiveAMOTL1 · rs2895570
See detailed info → Sensitivenear MTAP · rs74903566
See detailed info →Showing 20 of 146 · page 3 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.