Your Cart is Empty
Our Tests
12,000+
Patients cared for across Australia
500+
Doctors engaged
90%+
Patient satisfaction rate
Your partner in helping patients navigate the genomics landscape
We provide accredited genetic counselling and medical-grade genetic screening with end-to-end support for you and your patients every step of the way.
With Eugene as your partner, it’s easy to integrate genetic testing and counselling services into your practice.
Our services
Pregnancy care
Reproductive Carrier Screening is increasingly becoming a routine practice in preconception and prenatal care. RANZCOG & RACGP recommend that information about reproductive carrier screening be offered to all women, either prior to conception or in early pregnancy.
Eugene provides you and your patients with a streamlined service that combines diagnostic grade screening panels and accredited genetic counselling to ensure your patients can make informed and empowered pregnancy choices.
Preventative health
Preventative genetic testing for cancer and heart disease offers numerous benefits, including access to medicare funded programs for early detection, informed decision making, family risk assessment, and psychological support for patients.
By integrating Eugene into your practice, we make it easy for you to deliver a proactive and personalised approach to long-term patient care, ultimately improving patient outcomes.
Clinical snapshot of carrier screening
Core
Who
for females
(biological females screened first)
3 genes screened
(2 AR, 1 X-linked)
Conditions
Cystic fibrosis (CF) spinal muscular atrophy (SMA) and fragile X syndrome (FXS)
What
5% of females will be a carrier of CF, SMA or FXS. If female is a carrier of CF or SMA, male partner testing is recommended (medicare available).
1 in 240 couples will be at increased risk
Cost
$0 (if medicare eligible)
Collection method
at-home cheek swab collection kit
Turn around time
Results within 4 weeks
Comprehensive
Who
for individuals, reproductive couples and individuals using a donor
787 genes screened
(714 AR, 73 X-linked)
Conditions
Screens for 100s of genetic conditions relevant to more ethnicities (inc. CF, SMA and FXS). Includes conditions with severe and or significant impact on childhood health or development
What
Individual carrier results reported
~80% of individuals are healthy carriers
~1 in 35 couples will be at increased risk
Cost
$949 Individual
$1399 Couple
Collection method
at-home saliva collection kit
Turn around time
Results within 4 weeks
Couples
Who
reproductive couples only
(must include 1 person of female sex and 1 person of male sex)
629 genes screened
(559 AR, 70 X-linked)
Conditions
Screens for 100s of genetic conditions relevant to more ethnicities (inc. CF, SMA and FXS). Focuses on severe childhood onset conditions
What
Results are reported for a reproductive couple (Female carrier results for CF, SMA and FXS only)
~1 in 50 couples will be at increased risk
Cost:
$949 (if medicare eligible)
Collection method
at-home cheek swab collection kit
Turn around time
Results in 6 - 8 weeks
About the carrier test panel
A testing panel of up to 787 serious and actionable conditions.
We use three panels that include up to 787 autosomal recessive and X-linked conditions, including Cystic Fibrosis, Spinal Muscular Atrophy, Fragile X syndrome, Thalassaemia, and Tay-Sachs disease. These conditions are serious, actionable and relevant for patients to know about.
1. It’s comprehensive
When combined, the average risk of having a child with one of these conditions is higher than the risk of having a child with Down syndrome.
2. It’s actionable
Conditions that impact a child’s life expectancy or development & have limited treatment — where the knowledge of your risk can give you options.
3. It’s inclusive to all
Our test includes many serious conditions that are more common in different ethnic communities and are often excluded in industry standard tests.
Clinical snapshot of proactive health
Cancer Risk Test
65 genes
- BRCA1 & BRCA2 - Breast, ovarian, pancreatic, prostate cancer and melanoma.
- MLH1, MHS2, MSH6 & PMS2 - Lynch Syndrome: bowel, ovarian and uterine cancer.
- Turn-around time: 4-6 weeks
- Sample type: Saliva
- Sample processed in: USA
Genetic counselling:
Genetic counselling is included for every patient with before, during and after hour secure video consultation.
Lab results:
Internationally accredited, medically actionable.
Methodology:
Full-gene sequencing and deletion / duplication analysis using next-generation sequencing technology.
Not for diagnostic purposes or treatment options of a current diagnosis (VUS not reported).
Patient pay price:
$795 for individuals
Heart Health Test
83 genes
- MYBPC3, MYH7, FHL1 - Cardiomyopathy
- ACVRL1, BMPR2, ENG, GDF2, SERPINC1, SMAD4 - High blood pressure
- Turn-around time: 4-6 weeks
- Sample type: Saliva
- Sample processed in: USA
Genetic counselling:
Genetic counselling is included for every patient with before, during and after hour secure video consultation.
Lab results:
Internationally accredited, medically actionable.
Methodology:
Full-gene sequencing and deletion / duplication analysis using next-generation sequencing technology.
Not for diagnostic purposes or treatment options of a current diagnosis (VUS not reported).
Patient pay price:
$795 for individuals
Preventive Health Test
167 genes
- Everything in Cancer risk test
- Everything in Heart health test
- 19 additional risk genes, including CACNA1S, RYR1, SERPINA1 surgical risks
- Turn-around time: 4-6 weeks
- Sample type: Saliva
- Sample processed in: USA
Genetic counselling:
Genetic counselling is included for every patient with before, during and after hour secure video consultation.
Lab results:
Internationally accredited, medically actionable.
Methodology:
Full-gene sequencing and deletion / duplication analysis using next-generation sequencing technology.
Not for diagnostic purposes or treatment options of a current diagnosis (VUS not reported).
Patient pay price:
$1199 for individuals
Accessible nationwide
We provide an end-to-end service Australia and New Zealand wide
Clinical grade service
You get accredited lab results, Eugene reports and fully informed patients
Genetic education & counselling
Every patient gets access to pre-test education and post-test genetic counselling from qualified GCs
Integrates into your practice
Send referrals and get reports within your clinical systems and workflow
Meet the team
Genetics experts
Zoë Milgrom
Chief Clinical Officer & Genetic Counsellor
Prof. David Amor
MBBS, FRACP, PhD
Medical Director & Clinical Geneticist
Ari Horton
MBBS (hons) FRACP FCSANZ
Cardiologist & Genetics Fellow
Prof. Ingrid Winship
Professor of Genetics
Annabelle Kerr
Genetic Counsellor
Erin Macaulay
Genetic Counsellor
Ellie Greenberg
Assoc. Genetic Counsellor