Other applications using/annotating CADD

  • gnomAd: variants from population studies (15k WGS on GRCh37, 60k WGS on GRCh38)
  • Bravo/TOPMed: variants from WGS variant calls for currently ~60k people from GWAS studies
  • Ensembl VEP: genome variant annotation platform
  • dbNSFP: database for many different annotations
  • PopViz: webserver for visualizing minor allele frequencies and damage prediction scores of human genetic variations


This section primarily covers annotations that have been added since the v1.4 release. For more information about older annotations please see our manuscript.

GRCh38 specific