This product is only meant for customers who already purchased a MyGenome Test

Carrier Screening is a multi-gene panel aimed at investigating the probability of transmission of a genetic disease from parents to children. For this reason, the Carrier Screening Panel is suitable for couples who are planning a pregnancy and want to know the risk of transmitting hereditary diseases to their offspring. In fact, each of us can be an unconscious (since asymptomatic) carrier of mutations that can cause the onset of a congenital disease, based on the pattern of inheritance.

The potential of this test is high: the discovery of being a "carrier" (i.e. carrier) of certain mutations can in fact help the couple to monitor the pregnancy in an optimal way, possibly planning to undergo more invasive analyzes for prenatal diagnosis.

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 300 genes responsible for the main hereditary diseases analyzed
• Investigates SNP and Indel mutations up to 150 bp

Conditions analyzed are:

• Joubert and Meckel Syndrome
• Methylmalonic Aciduria and Homocystinuria
• Bardet-Biedl Syndrome
• Alstrom Syndrome

Find out all the analyzed genes here