How a “common language” to share genetic variation can improve patient care When a doctor suspects their patient might have a genetic disease, they can test a person’s genome to find differences (variants) that might cause the symptoms. However, it can be challenging to find information about a variant and its associated knowledge. Not only are there huge volumes of information, but also institutions, knowledgebases, and other data sources store information differently. The GA4GH Genomics Knowle
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