Non-invasive prenatal testing (NIPT)
Non-invasive prenatal testing (NIPT)  can detect genetic material (DNA) from the placenta in a blood test from the mother and screen for chromosomal abnormalities in the developing baby.
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Generation

Screening for common chromosomal changes in the fetus.

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$
455
Generation 46

Screening all chromosomes for changes in the fetus.

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$
525
Generation Plus

Screening for common chromosomal changes plus specific microdeletion syndromes in the fetus.

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$
799
Expanded Genetic Carrier Screening
Genetic carrier screening tests for gene changes in parents that when inherited by their children, may cause severe or life-threatening genetic conditions. Expanded carrier screening tests for hundreds of inherited conditions.
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Expanded Carrier Screen – Couple’s test

Comprehensive carrier screening for over 600 genetic conditions - for couples.

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$
1350
Expanded Carrier Screen – Individual test

Comprehensive carrier screening for over 600 genetic conditions - for an individual.

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$
699
Pharmacogenomics (Personalised Medicine)
Testing your DNA to determine how quickly or slowly you metabolise (break down) medications can help your doctor to prescribe you the best medication at the right dose.
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PGx Multi

Broad pharmacogenomic test covering mental health, pain, cardiology and additional medications.

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$
197
Hereditary Breast and Ovarian Cancer
Testing for inherited cancer genes that increase your risk of having breast and ovarian cancer. Useful in prognosis, medical management and directing therapy.
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Breast/Ovarian Cancer Gene Panel – BRAoVO™

Genetic panel for assessing breast and ovarian cancer risk genes.

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$
449
BRAoVO™ Plus Cancer Gene Panel

Genetic panel for breast, ovarian, and colorectal cancer risk genes.

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$
575
Familial Cancer gene testing (HBOC)

Single gene test for known familial cancer gene variants.

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$
300
BRCA1 & BRCA2

Genetic test for cancer risk BRCA1 & BRCA2 genes.

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$
449
BRAoVO™ Genetic Testing & Counselling Package (GP Request)

BRAoVO genetic panel for breast and ovarian cancer risk assessment plus pre- and post-test counselling sessions.

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$
899
Colorectal cancer syndromes
Testing for inherited cancer genes that increase your risk of having colorectal cancer. Useful in prognosis, medical management and directing therapy.
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Lynch Syndrome Panel

Screens for variants in genes associated with an increased high risk of colorectal and endometrial cancers.

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$
479
FAP/MAP Panel

Screens for variants in Familial Adenomatous Polyposis genes.

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$
479
Familial Cancer gene testing (Colorectal cancer)

Genetic test for colorectal cancer risk in those with family history.

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$
300
Cardiology
Genetics is helping to uncover the inherited factors behind many heart conditions. Understanding these genetic risks allows for personalised care, early interventions, and more effective management of heart disease for patients and their families.
Familial hypercholesterolaemia

Testing for genetic changes that cause high LDL cholesterol, increasing early CHD risk.

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$
599