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.
EXOC2 · rs9392026
See detailed info → SensitiveFOXP1 · rs35540156
See detailed info → SensitiveRHOU · rs801108
See detailed info → SensitiveFOXP1 · rs11708920
See detailed info → SensitiveAC017060.1 · rs17137933
See detailed info → SensitiveLOC101927630 · rs76128631
See detailed info → SensitiveST3GAL6 · rs7620634
See detailed info → SensitiveCHMP1A · rs35749174
See detailed info → SensitiveHLA-B · rs1050529
See detailed info → SensitiveTNS3 · rs7776701
See detailed info → SensitiveOBFC1 · rs7907606
See detailed info → SensitiveZBTB10 · rs11993814
See detailed info → SensitiveGATA3 · rs73635312
See detailed info → SensitiveOCA2 · rs12916300
See detailed info → SensitiveFOXP1 · rs2116709
See detailed info → SensitiveCUX1 · rs73183643
See detailed info → SensitiveRHOU · rs61824911
See detailed info → SensitiveZFHX4 · rs10093547
See detailed info → SensitiveRGS22 · rs141115006
See detailed info → SensitivePLIN3 · rs10425559
See detailed info →Showing 20 of 146 · page 7 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.