Abstract
Here we describe MyGene2, Geno2MP, VariantMatcher, and Franklin;
databases that have made variant-level information together with
phenotype or phenotypic features available to researchers, clinicians,
health care providers and patients. Following in the footsteps of the
Matchmaker Exchange project that connects exome, genome, and phenotype
databases at the gene level, these databases plan to connect to each
other using Data Connect, a standard for discovery and search of
biomedical data from the Global Alliance for Genomics and Health
(GA4GH).
