• Carrier Screening Report - Dante Labs World
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This report does not include the Genome Sequencing test (to be purchased separately)

Carrier Screening Report

Carrier Screening Report

Dhs. 127.00 AED
Dhs. 127.00 AED
Sale Sold out

✔️ Add-on Report to your Genome Test

Carrier Screening

Pathologies with recessive transmission, in order to manifest themselves, require that both copies of the gene (one of maternal origin and one of paternal origin) are mutated. The carriers of a single mutated gene are asymptomatic subjects unaware of having it. If, however, both subjects of the couple are carriers of the same mutated gene, there is a 25% chance, with each pregnancy, that a sick child will be born. Carrier screening is therefore an important tool for knowing one's carrier status.

More than 100 genes analyzed


It is recommended if:

This report is particularly suitable for couples who are planning a pregnancy and who want to have information on their possible carrier status. This awareness, in the event that both members of the couple have mutations on the same gene, facilitates the informed decision-making process, planning the best possible interventions and management strategies of a hypothetical pathological status transmitted to the offspring.


List of main conditions:

  • Usher syndrome
  • GRACILE syndrome
  • Muscular Dystrophy-Dystroglycanopathy
  • Alpha-1 antitrypsin deficiency
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Your blueprint for a healthier life

  • Actionable Insights

    Receive a complete blueprint to anticipate health risks years before symptoms appear, get a personalized prevention plan and make informed choices for a longer, healthier life

  • Your full DNA

    Get the full picture, not a snapshot. The genome is your full DNA and has 10,000 times more data than most wellness and ancestry DNA tests that analyze less than 0.01% of your DNA.

  • A lifelong investment

    Your DNA never changes, but science advances exponentially. Receive updates whenever new discoveries emerge—no need for repeated tests. Today's investment is tomorrow's insight

Thousands of lives transformed by the Dante Genome

Join the thousands whose life was transformed by the Dante Genome.

Better medical support, better clinical insights, real action plans, a new tool for your doctor

Why Dante

  • Superior Health Insights

    You receive actionable insights and a plan to take real steps in your life. Our reports provide real guidance on how to improve your healt and well being

  • Deeper Science

    From rare diseases to neurology, from longevity to family planning. Our sceince and expertise help solve more problems. Our reports cover a wide range of health uses

  • 10,000 Times More Data

    Unlock the power of 100% of your DNA. The genome has 10,000 times more data than most wellness and ancestry DNA test that analyze less than 0.01% of your DNA

Superior Insights

  • Fully personalized reports
  • Actionable insights
  • Genetic counseling (extra)
  • Proactive screening report
  • Future updates
  • Simple sample collection kit
  • Free worldwide shipping
  • 30X Coverage
  • Full ownership of your data
  • GDPR privacy protection

Deeper Science

  • 1 Million Genomic Reports

    We generated more than 1.3 million genomic reports based on whole genome delivering superior results to users in 100 different countries

  • AI Powered Interpretation

    From the AI Genome Chat to our automated updates, the Dante Genome offers actionable health insights across your entire body

  • State-of-the-art Sequencing Lab

    We run a clinical multiomics sequencing lab with ISO9001 accreditation and multiple Next Generation Sequencing workflows

10,000 times more data

  • The Dante Genome Test

    Whole genome sequencing is the analysis of your full DNA - 100% of your DNA - the most complete and comprehensive and complex DNA test available.

    We provide whole genome sequencing and generate and analyze 10,000 times more data than traditional genetic tests that only analyze less than 0.01% of your DNA.

  • Traditional DNA Tests

    Traditionally, genetic tests are limited to examining specific genes or regions of the genome, missing more than 99.9% of your DNA.

    These inferior DNA tests are based on an old technology called microarray but provide only limited insights.

FAQ

What is included in the test?

You receive your full whole genome data (FASTQ, BAM and VCF files), and AI reports. You can get additional reports anytime, without the need to re-send your sample.

What is 30X coverage?

30X coverage is the gold standard in clinical grade whole genome sequencing, offering high-confidence variant calls and interpretation. A 30X whole genome is a superior test than a low pass genome or a microarray

Will I get my raw data?

Yes - FASTQ, BAM, and VCF files are included

Who owns my DNA data?

You own your data. 100% of it. 100% of the time.

How do I collect my sample?

You will receive a saliva sample collection kit at home. Painless. Non invasive. Easy to use. And also a prepaid return label to send the sample back to our lab

What about shipping?

Shipping is free. Everywhere in the world. You will receive a return label with your kit to send your sample back to our lab

Do you work with companies?

If you have an interesting project or would like to speak with our B2B Team, please contact us. We provide genomics and multi-omics services to universities, biotech companies, clinics and hospitals