The Australia genetic testing market size reached USD 390.00 Million in 2024. Looking forward, IMARC Group expects the market to reach USD 904.66 Million by 2033, exhibiting a growth rate (CAGR) of 9.80% during 2025-2033. The market is growing due to rising demand for personalized medicine, increased awareness of preventive healthcare, and advancements in genomic technologies. Government initiatives, expanded prenatal and newborn screening programs, and the popularity of direct-to-consumer (DTC) tests further propel growth. Lower sequencing costs and telehealth integration also contribute to market expansion.
Report Attribute
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Key Statistics
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Base Year
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2024 |
Forecast Years
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2025-2033
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Historical Years
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2019-2024
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Market Size in 2024 | USD 390.00 Million |
Market Forecast in 2033 | USD 904.66 Million |
Market Growth Rate 2025-2033 | 9.80% |
Rising Demand for Direct-to-Consumer (DTC) Genetic Testing
The significant growth in direct-to-consumer (DTC) genetic testing, driven by increasing consumer interest in personalized health insights is favoring the Australia genetic testing market growth. Companies have popularized at-home testing kits, allowing individuals to access ancestry, health predisposition, and wellness reports without medical referrals. Advances in next-generation sequencing (NGS) and reduced testing costs have further fueled adoption. Australians are increasingly proactive about preventive healthcare, seeking genetic insights for conditions including cancer risk, cardiovascular diseases, and pharmacogenomics. Cardiovascular disease (CVD) affects 1 in every 6 Australians, or more than 4.5 million individuals, and remains one of the country's major health issues. CVD causes 24% of all deaths, a death every 12 minutes, and causes over 1,500 daily hospital admissions, with an annual cost of USD 5 Billion to public hospitals, 11% of the total cost of admissions. The elevated rates of mortality in men, Aboriginal communities, and rural dwellers all highlight the growing need for the integration of genetic risk screening into Australia's preventive cardiovascular care. Additionally, telehealth integration has made it easier for consumers to consult healthcare professionals after receiving results, enhancing market accessibility. However, concerns over data privacy and regulatory oversight remain challenges. The Therapeutic Goods Administration (TGA) is tightening guidelines to ensure test accuracy and ethical data handling, expanding the Australia genetic testing market share.
Expansion of Prenatal and Newborn Genetic Screening
Prenatal and newborn genetic testing is rapidly expanding in Australia, driven by advancements in non-invasive prenatal testing (NIPT) and government-backed screening programs. NIPT, which analyzes fetal DNA from maternal blood, is gaining traction due to its accuracy and safety compared to traditional invasive methods such as amniocentesis. Public and private healthcare providers are increasingly offering comprehensive carrier screening for conditions including cystic fibrosis and spinal muscular atrophy. Cystic fibrosis (CF) is a serious hereditary disorder affecting over 600 individuals in New Zealand, caused by mutations within the CFTR gene, mainly the F508del mutation, which occurs in around 90% of cases in the area. The condition is inherited when both parents carry the faulty gene, resulting in a 25% chance of their child being born with CF. Due to early diagnosis and improved treatment modalities, the outlook for individuals with CF is increasingly positive, and this emphasizes the importance of genetic screening and carrier testing in Australia's preventive health system. Additionally, state-funded newborn screening programs now include broader genetic panels for early detection of metabolic and genetic disorders. The growing emphasis on early intervention and personalized pediatric care is enhancing demand. However, ethical considerations around genetic data storage and informed consent persist. As genomic research progresses, Australia is integrating more extensive genetic screening into standard prenatal and neonatal care, further creating a positive Australia genetic testing market outlook.
IMARC Group provides an analysis of the key trends in each segment of the market, along with forecasts at the county and regional levels for 2025-2033. Our report has categorized the market based on type, technology, and application.
Type Insights:
The report has provided a detailed breakup and analysis of the market based on the type. This includes predictive and presymptomatic testing, carrier testing, prenatal and newborn testing, diagnostic testing, pharmacogenomic testing, and others.
Technology Insights:
A detailed breakup and analysis of the market based on the technology have also been provided in the report. This includes cytogenetic testing and chromosome analysis, biochemical testing, and molecular testing (DNA sequencing and others).
Application Insights:
The report has provided a detailed breakup and analysis of the market based on the application. This includes cancer diagnosis, genetic disease diagnosis, cardiovascular disease diagnosis, and others.
Regional Insights:
The report has also provided a comprehensive analysis of all the major regional markets, which include Australia Capital Territory & New South Wales, Victoria & Tasmania, Queensland, Northern Territory & Southern Australia, and Western Australia.
The market research report has also provided a comprehensive analysis of the competitive landscape. Competitive analysis such as market structure, key player positioning, top winning strategies, competitive dashboard, and company evaluation quadrant has been covered in the report. Also, detailed profiles of all major companies have been provided.
Report Features | Details |
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Base Year of the Analysis | 2024 |
Historical Period | 2019-2024 |
Forecast Period | 2025-2033 |
Units | Million USD |
Scope of the Report |
Exploration of Historical Trends and Market Outlook, Industry Catalysts and Challenges, Segment-Wise Historical and Future Market Assessment:
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Types Covered | Predictive and Presymptomatic Testing, Carrier Testing, Prenatal and Newborn Testing, Diagnostic Testing, Pharmacogenomic Testing, Others |
Technologies Covered |
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Applications Covered | Cancer Diagnosis, Genetic Disease Diagnosis, Cardiovascular Disease Diagnosis, Others |
Regions Covered | Australia Capital Territory & New South Wales, Victoria & Tasmania, Queensland, Northern Territory & Southern Australia, Western Australia |
Customization Scope | 10% Free Customization |
Post-Sale Analyst Support | 10-12 Weeks |
Delivery Format | PDF and Excel through Email (We can also provide the editable version of the report in PPT/Word format on special request) |
Key Questions Answered in This Report:
Key Benefits for Stakeholders: