The human genome holds a promise: complete understanding of human disease. Unfortunately, this promise is locked because critical data and knowledge are being hoarded. This is delaying progress.
It’s time to restore the balance between open science and commercial interests. With AmbryShare, we can break the mold to unlock the promise of the human genome.
Explore our AmbryShare database and download aggregated cohort data for free by registering. This allows you to search for alterations, review allele frequency within our disease cohorts, and access links to other publicly available disease and variant specific databases. We will also send updates on AmbryShare and any new disease cohort/aggregate data as they are available.