VarSeq Software

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VSClinical allows for the clinical interpretation of variants based on ACMG & AMP Guidelines

The VSClinical guided workflow enables following the American College of Medical Genetics (ACMG) guidelines used to identify and classify causal variants for inherited disease risk, cancer predisposition and the diagnosis of rare diseases.

As an optional add-on, VSClinical can follow the Association for Molecular Pathology (AMP) guidelines used for performing targeted cancer gene panel tests popular in molecular pathology labs to report significant biomarkers of clinical utility in precision medicine.

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VarSeq ® Software is intended for Investigational Use Only. The performance characteristics of this product have not been established.