Genetic compatibility carrier test
- FIND OUT if you are a carrier of a genetic disease that could affect your offspring.
- CHECK your genetic compatibility with your partner before pregnancy.
- PREVENT serious genetic diseases in your children.
Genetic compatibility carrier test
550,00 €
Who is the test for?
The test is aimed at:
- Especially to those couples with a family history of hereditary diseases.
- To couples who want to try to get pregnant naturally.
- To couples or women who want to opt for assisted reproduction treatments.
- To couples or women who require gamete donation in order to select the most suitable donor.
- Consanguineous couples.
Genetic diseases have no cure, but they can be prevented.
What results can I get?
- Negative genetic matching : the partners do not have genetic mutations in the same gene. No risk of transmitting the diseases included in the study is identified.
- Positive genetic matching : Both partners carry mutations in the same gene and are therefore carriers of the same disease. They have a 25% chance of having affected offspring. This occurs in 5% of couples.
Do you have any questions?
We recommend that you request a free first visit so that our doctors can learn about your case and answer your questions.
How does it work?
1. Sample extraction in one of our centers
After purchasing the carrier test, we will schedule an appointment at your nearest center (see our network of centers here ), and we will provide you with the document you must bring to the appointment.
2. Gene analysis and results in 20 days
Your results will be available by email. If you take the test as a couple, you will receive two reports: the individual report and the couple matching report.
3. Visit to explain results
After receiving the report, you can request the results explanation visit included in the test. This visit is conducted online with one of our doctors.
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0
recessive genes
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0
X-linked genes
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0
detected diseases
Object of study
What diseases and genes are included?
- 470 recessive genes
- 66 genes linked to the X chromosome
- +500 affected diseases
You can see the complete list of genes and diseases included here .
Our test is compatible with all other tests on the market. The technology we use allows us to add genes based on family history.
The test can be taken individually or in pairs.
— Our Commitment
Rigor, quality, and technology
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We only analyze variants with solid scientific evidence
Our expert panel selects and reviews variants with solid scientific evidence based on scientific literature and medical guidelines.
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Quality Assurance
The laboratory where samples are processed and analyzed holds ISO 15189 and 9001 certifications.
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We use the best technology available
We use the PMDA (Precision Medicine Diversity Array) platform by Applied BioSystems, which enables the analysis of over 850,000 genetic markers in your DNA with a quality rate over 99%. It is the most comprehensive platform on the market, designed to cover all relevant genetic variants related to your health. This platform includes genetic variants from all ancestral populations and also provides analysis of specific mitochondrial DNA and Y chromosome markers, allowing for a deeper and more accurate understanding of your ancestral origins.
— Do you have any more questions?
Ask us your questions
Call us at +34 93 115 99 50, send us a message on WhatsApp, or fill out the form below: