• Lynch Syndrome Report
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Lynch Syndrome Report

Lynch Syndrome Report

€19,00 EUR
€19,00 EUR
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The Lynch syndrome test is based on Whole Genome Sequencing Test. As such, it analyzes all Common and Rare Variants associated with Lynch syndrome instead of a limited set of genes. Lynch syndrome, often called hereditary nonpolyposis colorectal cancer (HNPCC), is an inherited disorder that increases the risk of many types of cancer, particularly cancers of the colon (large intestine) and rectum, which are collectively referred to as colorectal cancer. People with Lynch syndrome also have an increased risk of cancers of the stomach, small intestine, liver, gallbladder ducts, urinary tract, brain, and skin. Additionally, women with this disorder have a high risk of cancer of the ovaries and lining of the uterus (endometrial cancer). Women with Lynch syndrome have a higher overall risk of developing cancer than men with the condition because of these cancers of the female reproductive system. Individuals with Lynch syndrome typically develop cancer in their forties or fifties. Along with environmental factors, Genetics plays a key role in the regulation of Fibromyalgia. - 78 genes analyzed - 100% of genomic regions covered - Intragenic and intergenic regions analyzed - All variants reported

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What You Get

  • Wellness Report

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

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  • 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.

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  • 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.

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  • 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.

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How it works

  • 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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