Cutting edge, affordable
genetic testing for all Australians
At Genomic Diagnostics, we focus on leading the way in providing accessible, quality genetic testing answers to improve your health.
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.
Inherited genetic variants cause 5-10% of breast cancers.
Genomic testing can help guide patients to know their genetic risk.
For full details click HERE or contact us on 1800 822 999.
PGx is the study of genetic variations that influence medication response.
It can be used particularly in mental health to identify if patients:
Are at higher risk of side effects from their medication
Have higher potential for therapeutic failure
Are likely to expect symptom relief from a standard dose
Non-Invasive Prenatal
Testing
(NIPT)
- Generation
- Generation 46
- Generation Plus
Carrier
Screening
- Core Genetic Carrier Screen
- Expanded Genetic Carrier Screen
Inherited Disorders
- Familial Hypercholesterolaemia
- Haemochromatosis
- Factor V Leiden/Prothrombin
- Coeliac Risk
Oncology
- Hereditary Breast & Ovarian Cancer
- Tumor Molecular Testing
- Hereditary Colorectal Cancer
- Haematological 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.
Dedicated Australian customer care team
Direct access to our clinical and scientific team for health professionals
A leader in cutting-edge technology to improve health
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.
Part of the Healius Pathology network incorporating…
Leading the way to improved health
results in the shortest turnaround time.
