Empowering your
health decisions

Genomic risk assessment covering over 50 inherited conditions.
Medication analysis covering over 220 medications.
One-on-one genetic counselling.
Receive your personalised test report.
Managed by your doctor.
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GoExplore is a test that involves sequencing your genome – all of your DNA, including all of your genes.

The GoExplore advantage

Gain knowledge and information for the future

Each gene included in GoExplore™ is associated with a condition that can potentially be treated, managed, monitored or prevented

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Take the first step towards precision healthcare

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Knowing your risks can help you and your doctor make proactive health decisions by taking steps to detect diseases early, or even prevent them from developing

Understand your response to certain medications

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Information on how your genes affect your likely response to certain medications may help your doctor prescribe the most appropriate medications for you

Understand your genetic risk

  • GoExplore assesses your genetic risk of developing over 50 inherited conditions including inherited cancers and heart conditions

  • Knowing your risks can help you and your doctor make proactive health decisions by taking steps to detect diseases early, or even prevent them from developing

List of inherited conditions analysed by GoExplore


Birt-Hogg-Dubé syndrome

Bloom syndrome

Bowel cancer

Breast cancer

Cowden syndrome

Endometrial cancer

Familial adenomatous polyposis

Fanconi anaemia

Gastrointestinal stromal tumour

Gorlin syndrome

Hereditary diffuse gastric cancer

Hereditary leiomyomatosis and renal cell cancer

Hereditary paraganglioma-pheochromocytoma

Howel-Evans syndrome

Juvenile polyposis syndrome / hereditary mixed polyposis syndrome

Li-Fraumeni syndrome

Lynch syndrome



Multiple endocrine neoplasia


Ovarian cancer

Pancreatic cancer

Papillary renal cell cancer

Peutz-Jeghers syndrome

Prostate cancer


Rhabdoid tumour predisposition syndrome

Tumour predisposition syndrome

Von Hippel-Lindau syndrome

Wilms tumour

Heart conditions


Arrhythmogenic right ventricular cardiomyopathy

Atrial fibrillation

Brugada syndrome

Catecholaminergic polymorphic ventricular tachycardia

Dilated cardiomyopathy

Familial hypercholesterolaemia

Hypertrophic cardiomyopathy

Left ventricular noncompaction

Long QT syndrome

Pulmonary hypertension

Short QT syndrome

Structural heart defects

Other inherited conditions

Malignant hyperthermia

Ornithine transcarbamylase deficiency

Periodic paralysis

Tuberous sclerosis

Wilson’s disease

Learn how you respond to medication

  • GoExplore gives you insights into how your genes affect your likely response to over 220 medications used for many conditions

  • This information may help your doctor prescribe the most appropriate medications for you

List of conditions

Acute migraine



Alzheimer’s disease


Antiplatelet therapy



Bacterial infection

Benign prostatic hyperplasia


Chronic hepatitis C




Fungal infection

Gastroesophageal reflux disease


HIV infection



Migraine prophylaxis

Overactive bladder


Parkinson’s disease


Rheumatoid arthritis


Sleep disorders

Smoking cessation

Receive ongoing expert support

  • After you are referred for testing by a doctor, our will walk you through the testing process and what the potential results could mean for you and your family

  • After testing, our experts will help you understand your results and any actions you can take

Our genetic health professionals

profile picture of Mary-Anne Young
Genetic Counsellor
profile picture of Ebony Richardson
Genetic Counsellor

Health is complex. Your lifestyle, your environment and the information encoded in your DNA all interact to influence your health. Personal health genomics analyses your genome (the entirety of a person’s genetic material including all their genes) to provide you with a genomic profile. This profile can help you and your doctor to make personalised health decisions.

GoNavigate is a collaboration between Genome.One and LifeFirst. LifeFirst has been developed from the success and knowledge of its parent company, Executive Health Solutions (EHS). EHS has been a leading provider of executive health and wellbeing programs in Australia for more than 30 years having completed around 100,000 detailed health screens since its inception within the St Vincent’s Hospital precinct in Sydney.

How it works

See your doctor

Your doctor can refer you to Genome.One for genetic counselling.

Have genetic counselling

Make an appointment to meet our genetic health professional to discuss any questions you may have.

Give sample

After you have decided to go ahead, provide a blood sample for testing.

Receive results

After analysis has been completed (approximately 8-12 weeks), meet our genetic health professionals again to learn about your results.

Follow up

Based on your results, we will support your doctor in recommending steps to manage your health.

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Contact details

1300 466 631

370 Victoria St, Darlinghurst NSW
2010, Australia