Carrier screening analysis is a genetic test that assesses an individual’s carrier status for specific genetic conditions, particularly those associated with recessive disorders. Carriers are individuals who carry a single copy of a mutated gene but do not typically display symptoms of the associated disorder. These conditions often require two copies of the mutated gene (one from each parent) for the disorder to manifest in the offspring
The importance of carrier screening lies in its ability to provide individuals or couples with information about their risk of passing on genetic disorders to their children.
With a commitment to excellence, Savyon’s professional team of sequencing specialists and human genetic experts ensures the highest standards in carrier screening.
Partner with us to provide your customer with the best offered analysis to allow for informed choices and early intervention to manage or prevent the impact of genetic disorders in future generations.
