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Sjögren’s Syndrome Panel

Sjögren’s Syndrome Panel

Regular price €49.00 EUR
Regular price Sale price €49.00 EUR
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The Sjögren’s Syndrome test is based on the Whole Genome Sequencing Test. As such, it analyses all Common and Rare Variants associated with Sjögren’s Syndrome instead of a limited set of genes. Sjögren's syndrome is an autoimmune disease. This means that your immune system attacks parts of your own body by mistake. In Sjögren's syndrome, it attacks the glands that make tears and saliva. This causes a dry mouth and dry eyes. You may have dryness in other places that need moisture, such as your nose, throat, and skin. Sjögren's can also affect other parts of the body, such as your joints, lungs, kidneys, blood vessels, digestive organs, and nerves. Along with environmental factors, Genetics plays a key role in the regulation of Sjögren’s Syndrome. - 11 genes analyzed - 100% of genomic regions covered - Intragenic and intergenic regions analyzed - All variants paneled.


Click here to see all the genes analyzed

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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