Clinical Interpretation of genetic variants by ACMG/AMP 2015 guideline

InterVar is a bioinformatics software tool for clinical interpretation of genetic variants by the ACMG/AMP 2015 guideline. The input to InterVar is an annotated file generated from ANNOVAR, while the output of InterVar is the classification of variants into 'Benign', 'Likely benign', 'Uncertain significance', 'Likely pathogenic' and 'Pathogenic', together with detailed evidence code.

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Dr. Quan Li

Zilkha Neurogenetic Institute
Keck School of Medicine
University of Southern California(USC)
CV / Web: http://www.quanli.org/
Email: jeele@ustc.edu or leequan@gmail.com
Google Scholar and Research Gate
Current: Princess Margaret Cancer Centre,University Health Network(UHN), University of Toronto,Canada
Faculty of Medicine, Memorial University of Newfoundland(MUN), Canada

Dr. Kai Wang

Associate Professor
Zilkha Neurogenetic Institute
Keck School of Medicine
University of Southern California(USC)
Web: http://wglab.org/
Email:kaichop@gmail.com
Current: Department of Pathology and Laboratory Medicine,University of Pennsylvania(Upenn),USA