OpenCravat integrates several key databases that are crucial for cancer research:
ClinVar: Provides information on the clinical significance of genetic variants. dbSNP: A comprehensive resource for single nucleotide polymorphisms (SNPs). COSMIC: The Catalogue of Somatic Mutations in Cancer, which offers extensive data on somatic mutations found in cancer. GnomAD: Contains data on population allele frequencies, helping to distinguish between common and rare variants.
