Carrier Screening Panel
Carrier Screening Panel
Regular price
€29.00 EUR
Regular price
Sale price
€29.00 EUR
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This product is only meant for customers who already purchased a MyGenome Test
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.
This panel 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.
The analysis takes into consideration the mutation of germline DNA, it investigates SNP and Indel mutations up to 150 bp.
List of main conditions:
Learn More
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.
This panel 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.
The analysis takes into consideration the mutation of germline DNA, it investigates SNP and Indel mutations up to 150 bp.
- Available in less than 24 hours
- Based on Whole Genome Sequencing
- More than 100 genes analyzed
- Investigates SNP and Indel mutations up to 150 bp
List of main conditions:
- Usher syndrome
- GRACILE syndrome
- Muscular Dystrophy-Dystroglycanopathy
- Alpha-1 antitrypsin deficiency
This product is only meant for customers who already purchased a MyGenome Test