Cutting edge, affordable
genetic testing for all Australians

Non-invasive prenatal testing (NIPT) Australia

The Generation non-invasive prenatal test (NIPT) screens for the most common chromosomal abnormalities that can affect your baby’s future health using a simple blood test.

Generation 46 NIPT Australia

Familial hypercholesterolaemia (FH) is a genetic disorder characterised by very high levels of LDL cholesterol, leading to an increased risk for coronary heart disease at an early age.

Genomic testing is the gold standard for diagnosis and management of FH. Our extended gene panel includes testing of 9 genes to achieve improved diagnostic efficiency over smaller panels.

Breast & Ovarian Cancer Screening

Guide your patients and know their genetic risk.
Our comprehensive gene panel test for breast cancer risk, the BraOVO test, is now available for $399.
Bulk billing is available for patients who meet MBS criteria.

Analysing thousands of genetic markers, this non-invasive test can be performed from 7 weeks gestation. Available for $1599 with the added flexibility of Latitude Pay.

Non-Invasive Prenatal
Testing (NIPT)
Carrier
Screening
Pharmacogenomics
Paternity, Relationship
& Immigration
Inherited Disorders
Oncology

Exceptional customer service, supported by a dedicated team.

At Genomic Diagnostics, we never lose sight of the person behind each test, which is why we look to personalise your experience.

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Dedicated Australian customer care team

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Direct access to our clinical and scientific team for health professionals

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A leader in cutting-edge technology to improve health

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Around 2,000 collection centres in all major cities and regionally nationwide

How it works

Accessing genetic testing is simple, and most of the time all we need is a blood sample or a cheek swab. With medical genetic testing, you will need to see your  doctor first to discuss whether the test is right for you and to organise a referral form.

2. Prepare for your collection

Some genetic and genomic tests may need prepayment, or may need specialised counselling, or documentation. Depending on the test, counselling might occur before the test, or after the result. For some tests where counselling occurs before a test, a consent form may need to be signed. Relationship testing may need proof of identity.

4. See your doctor to get your results

Your result is provided to your doctor, who will discuss this with you and action any relevant findings.

1. See your doctor to get a referral

Genetic and genomic testing can provide important health information that can make a diagnosis, inform treatment or management, or identify a health risk. See your doctor, who can discuss the appropriate test with you, and request the test. Non-medical tests (such as paternity and relationship testing) do not need a medical referral.

2. Prepare for your collection

Some genetic and genomic tests may need prepayment, or may need specialised counselling, or documentation. Depending on the test, counselling might occur before the test, or after the result. For some tests where counselling occurs before a test, a consent form may need to be signed. Relationship testing may need proof of identity.

3. Get your sample collected

Your doctor will provide you with a request form for testing. You can have your sample collected at one of our collection centres. Your sample is then transported to the laboratory, and tested.

4. See your doctor to get your results

Your result is provided to your doctor, who will discuss this with you and action any relevant findings.

We’re Australia-wide

Our footprint spans nationwide through our network of pathology partners, making testing more accessible for you.

Genomic Diagnostics locations

Part of the Healius Pathology network incorporating…

Leading the way to improved health

Our dedicated team are committed to ensuring the best quality
results in the shortest turnaround time.