What is the Genetic Carrier Screening test?
Genetic Carrier Screening helps identify if you carry a gene for an inherited condition that could be passed on to your child.
While everyone carries at least one genetic condition, most people are healthy and may not realise they carry a gene or how it could impact their children. Expanded carrier screening typically checks for more than 150 conditions, providing much more insight than standard tests, which usually focus on only three common conditions.
Why should you consider getting tested?
Genetic testing is the only way to find out whether or not you are a carrier for one of these conditions.
Knowing your carrier status can help you make informed choices. For many people, genetic carrier screening provides peace of mind. For those with a higher risk of having an affected child, it provides the opportunity to consider a range of options.
If you are found to be carriers of a condition, there are several reproductive options you can discuss with your doctor including:
- natural pregnancy, with or without prenatal diagnosis
- preimplantation genetic diagnosis with in vitro fertilisation (IVF) to test and then transfer embryos that are free of the condition
- the use of a sperm or egg donor
- adoption
Introducing the Natera Horizon expanded carrier screen
At Genomic Diagnostics, we offer the Natera Horizon expanded carrier screen, which can detect over 600 conditions in females and 550 in males. This highly accurate test gives you quality results in just 3-4 weeks from the time your sample is received at the lab.
You can choose to take the test individually or with your partner, based on your needs.
To support you throughout the process, we include free pre- and post-test genetic information sessions, and if you’re at higher risk, we also offer in-depth genetic counselling.
Our dedicated Customer Care Team is available to answer any questions you may have, ensuring you feel supported at every step.
