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Cardiovascular Report

Cardiovascular Report

Regular price €19,00 EUR
Regular price €49,00 EUR Sale price €19,00 EUR
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The Cardiovascular Report is based on Whole Genome Sequencing Test. As such, it analyzes all Common and Rare Variants associated with Cardiovascular Diseases instead of a limited set of genes, like old genetic target panels.

The Cardiovascular Report analyzes over 6000 conditions giving you insights into the following heart-related diseases:

  • Arrhythmogenic right ventricular cardiomyopathy
  • Brugada syndrome
  • Thoracic aortic aneurysm and aortic dissection
  • Hypertrophic cardiomyopathy
  • Long QT syndrome
  • Familial hypercholesterolemia
  • Wolff-Parkinson-White pattern
  • Atrioventricular septal defect
  • Familial Hypertrophic Cardiomyopathy
  • and many more heart-related diseases 

Along with environmental factors, Genetics plays a key role in the etiology of several forms of Cardiovascular Diseases.

  • More than 340 genes analyzed
  • 100% genomic regions covered
  • Intragenic and intergenic regions analyzed
  • All variants reported


See more about the product
  • Wellness Report

    The Wellness Report clarifies which habits are best suited to your genome, with actionable insights to live a better life.

    See a report 
  • Scientific Fitness Report

    The Fitness report gives you actionable advice on training, sports, fitness and physical activity. This will help you develop the right workout for you based on your whole genome.

    See a report 
  • Nutrigenomics Report

    Learn about the relationships between food groups and your genes. Using this report, you can create the most effective and personalized diet with a specialist.

    See a report 
  • Health and Predispositions

    Learn more about your risk to develop +50 diseases and conditions. Start taking a proactive approach to your health with our actionable insights.

    See the report 
  • 1.

    Using a simple at home blood sample, we can collect the 100% of your DNA and analyze the genetic sequence in our lab.

  • 2.

    The sequence is divided into several parts, amplified, grouped in clusters and then sequenced.

  • 3.

    This sequencing process reveals the order of nucleotides that make up the original DNA sample.

  • 4.

    We then compare the genome with a generic and globally recognized reference DNA sequence.

Simple Blood Sample Collection

Painless, quick at home sample collection. User friendly device with CE-IVD mark and FDA approval.

Simply follow the packaging instructions and send the sample back using the pre-paid returns label.

Genomic Consultation Service

Additional reports

Check out the full range of our additional reports, available upon completion of the Genome Test.

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