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Eugene Labs
The next step after carrier screening

Sequence - proactive genetic testing for your long-term health.

Screen for inherited cancer and heart health risks using the DNA you’ve already shared with Eugene.

  • Screens 180+ genes
  • No new sample required
  • Special pricing for Eugene Alumni
Eugene Labs

Know your risks before they become your reality

1 in 20 people carry an inherited health risk.

Many find out after it's too late for prevention. Finding an inherited risk isn’t a diagnosis. It’s early information that gives you time to act, adjust screening, and reduce your long-term risk.

Silent risks can

  • Be inherited, even without a known family history
  • Remain invisible in standard blood tests and MRIs
  • Appear without warning or symptoms

How results guide action

  • When screening starts and how often you’re monitored
  • Medication and preventive care choices
  • How you and your GP manage risk across your lifetime
Eugene Labs

Medical-grade testing, focused on what matters

Unlike other consumer DNA tests, Eugene does not report on traits or non-actionable findings. Every condition we screen for has established clinical relevance and clear next steps.

Benefits

  • Tested in accredited medical laboratories (CLIA, CAP), meeting rigorous clinical and quality standards.
  • We only test for genetic conditions that are medically important and actionable by clinicians.
  • Your data is protected using SOC 2 Type I & II security standards.
Eugene Labs

Eugene Alumni

If you’ve completed comprehensive carrier screening with Eugene, you can access proactive genetic health screening without a new sample.

We can use your existing DNA sequence to screen for inherited cancer and heart health risks, making this test faster, simpler, and available to you at a special alumni price.

What our test covers

Preventative Health

genes

These charts show the distribution of genes across health impact categories in our cancer, cardiac, and comprehensive preventative panels. The chart widths are proportional to each panel’s total genes.

This categorisation is based on the primary health impacts of each gene. Some genes influence multiple systems, but each is grouped by its single most clinically relevant impact.

Health Impact Categories

How it works

Four simple steps, expert analysis, and a personalised plan for your long-term wellness.

1

Order your test

Start your journey from the comfort of home

2

Share your story

Help us to make testing meaningful to you and your goals

3

Reanalysis

Your DNA sequence is reanalysed to uncover new health insights.

4

Review and guidance

Get a personal report, genetic telehealth consult and next steps

40,000+

Members across Australia

2000+

Doctors engaged

90%+

Customer satisfaction rate

Meet our genetics experts

Zoë Milgrom

Chief Clinical Officer & Genetic Counsellor

Prof. David Amor

Medical Director & Clinical Geneticist, MBBS, FRACP, PhD

Ari Horton

Cardiologist & Clinical Geneticist, MBBS (hons) FRACP FCSANZ

Rozanna Alli

Clinical Geneticist, FRACP MBBS BMedSci BBus

Erin Macaulay

Genetic Counsellor

Antonia Howard

Assoc. Genetic Counsellor

Frequently asked questions

Everything you need to know about Eugene Sequence