Learn to use GVS (Genome Variation Server), a comprehensive database that provides quick access to all data found in both the dbSNP and HapMap databases and includes specialized data from other projects. The database includes a suite of analysis tools such as linkage disequilibrium plots, tag SNPs, merging populations, and more. In addition you can upload our own data and use the GVS analysis and visualization tools. If your research involves genetic variation and SNPs, learn how to use this valuable tool for your analysis needs.
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Variation & Medical : Resources that include information about sequence variation, phenotypes, or medically-relevant conditions.
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Recent BioMed Central research articles citing this resource
van der Velde Joeri K. et al., GAVIN: Gene-Aware Variant INterpretation for medical sequencing. Genome Biology (2017) doi:10.1186/s13059-016-1141-7
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Yen L. Jennifer et al., A variant by any name: quantifying annotation discordance across tools and clinical databases. Genome Medicine (2017) doi:10.1186/s13073-016-0396-7