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Dante Non Invasive Prenatal Test

Dante Non Invasive Prenatal Test

€599,00 EUR
€599,00 EUR €599,00 EUR
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The Dante Labs Non-Invasive Prenatal Test (NIPT) is a reliable and safe genome analysis for expectant mothers to test for chromosomal abnormalities in their babies. This is a blood test that analyses the baby’s DNA, which circulates in the mother’s blood, using Next Generation Sequencing technology to detect and sequence the baby's circulating DNA. 

  • Our non-invasive testing method uses a small blood sample to make an accurate diagnosis of chromosomal conditions in your baby’s DNA.
  • The test involves 4 different kinds of comprehensive analyses that tests for genetic variations in your baby’s DNA.
  • Test for conditions such as Down Syndrome, Edward Syndrome and Turner Syndrome.
  • Understand your baby’s potential health conditions and plan in advance for any required care.
  • Access a comprehensive report that breaks down your baby’s chromosomal data.
  • Free worldwide shipping.
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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.

      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 

    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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      €599,00 EUR
      €599,00 EUR €599,00 EUR

    • Example product title

      €599,00 EUR
      €599,00 EUR €599,00 EUR

    • Example product title

      €599,00 EUR
      €599,00 EUR €599,00 EUR

    • Example product title

      €599,00 EUR
      €599,00 EUR €599,00 EUR
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