Skip to product information
1 of 2

Short QT Syndrome Panel

Short QT Syndrome Panel

Regular price €29.00 EUR
Regular price Sale price €29.00 EUR
Sale Sold out
This product is only meant for customers who already purchased a MyGenome Test

Short QT syndrome is a condition that can cause a disruption of the normal rhythm of the heart (arrhythmia). In people with this condition, the heart muscle (cardiac) takes less time than usual to recharge between beats.
Short QT syndrome is a rare genetic disorder that affects the heart's electrical activity. Short QT syndrome is caused by mutations in genes involved in the regulation of ion channels in the heart, and this panel tests for genetic variants that are known to affect these processes.
This panel is designed for individuals with a family history of short QT syndrome or individuals with symptoms of the condition, such as palpitations, syncope, and sudden cardiac arrest. Genetic testing can confirm a diagnosis, provide information on disease severity and progression, and inform treatment and management decisions. Testing can also inform family planning decisions and provide reassurance for unaffected family members.

The analysis takes into consideration the mutation of germline DNA, it investigates SNP and Indel mutations up to 150 bp.

  • Available in less than 24 hours
  • Based on Whole Genome Sequencing
  • 5 genes analyzed
  • Investigates SNP and Indel mutations up to 150 bp

List of main conditions:
  • Short QT Syndrome
Learn More
  • 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.

1 of 12
1 of 5