Welcome to dbHCCvar
dbHCCvar is an online database of human genetic variations whose association with hepatocellular carcinoma has been statistically investigated. It contains the human genetic variations which have been statistically tested to be associated or not associated with hepatocellular carcinoma risk, clinical pathology, drug reaction, survival or recurrence to date. dbHCCvar establishes a guaranteed updating system to add newly reported data in time. Till Sep 4, 2012, 820 entries referring to 636 unique human genetic variations are listed in dbHCCvar. It is expected that dbHCCvar will function as a useful tool for researchers to speed up the searching and identification of new human genetic markers for hepatocellular carcinoma. dbHCCvar is freely accessible for non-profit users.
Please cite:Xiaojia Y, Fang F, et al. dbHCCvar: a comprehensive database of human genetic variations in hepatocellular carcinoma. Hum Mutat. 2011, 32(12):E2308-16.
Disclaimer: We cannot guarantee that all the information in this database is accurate and latest.