An expanded carrier screening test that checks both partners for hidden (carrier) variants in genes linked to serious recessive inherited conditions.
Helps couples know their chance of having a child with conditions such as thalassaemia, spinal muscular atrophy or cystic fibrosis, ideally before or early in pregnancy, so they can plan with a genetic counsellor.
Suspected inherited conditions, family history, or as advised by a specialist or genetic counsellor.
No fasting needed.
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Yes. Genetic counselling before and after testing helps you understand the results and what they mean for you and your family.
No fasting is needed. You can eat and drink normally unless your doctor has advised otherwise.
Blood sample (EDTA tube); some genetic tests also accept saliva, tissue or other samples.
Usually within 31–32 days after the sample reaches the lab. You will receive the report online.