ABOUT THE PROJECT
Database for sharing genetic variants in hereditary cancer genes and their interpretation from expert panels and Spanish genetic diagnostics laboratories. The database also provides population frequencies of variants in Spanish individuals based on their clinical suspicion of cancer predisposition. The ultimate purpose of SpadaHC is to offer a useful resource for the research community and clinical genetic laboratories to improve the knowledge of the genetic basis of hereditary cancer and, therefore, to improve diagnosis, risk assessment, prevention, and cancer treatment of carriers and their families.
Find out more about SpadaHC in its own website.
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