Fig. 2From: Integrating 400 million variants from 80,000 human samples with extensive annotations: towards a knowledge base to analyze disease cohortsRVS web query interface: public datasets in RVS can be queried by coordinates (shown), dbSNP, genes, and by defining ‘cohorts’ using populations in RVS. RVS will return full annotations, frequencies, phenotypes, and literature referencesBack to article page