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US Carrier Screening Market

ID: MRFR/Pharma/15205-HCR
100 Pages
Garvit Vyas
October 2025

US Carrier Screening Market Research Report By Test Type (Single Gene Testing, Panel Testing, Expanded Carrier Screening), By Technology (Next Generation Sequencing, Polymerase Chain Reaction, Sanger Sequencing), By Application (Prenatal Screening, Preconception Screening, Newborn Screening) and By End User (Hospitals, Diagnostic Laboratories, Research Institutions) - Forecast to 2035

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US Carrier Screening Market Summary

As per MRFR analysis, the US carrier screening market Size was estimated at 1495.68 USD Million in 2024. The US carrier screening market is projected to grow from 1627.74 USD Million in 2025 to 3793.16 USD Million by 2035, exhibiting a compound annual growth rate (CAGR) of 8.83% during the forecast period 2025 - 2035.

Key Market Trends & Highlights

The US carrier screening market is experiencing robust growth driven by technological advancements and increasing awareness.

  • Technological advancements in genetic testing are enhancing the accuracy and efficiency of carrier screening processes.
  • The largest segment in the market is prenatal carrier screening, while the fastest-growing segment is expanded carrier screening.
  • There is a notable increase in awareness and demand for genetic counseling among prospective parents and healthcare providers.
  • Key market drivers include the rising prevalence of genetic disorders and advancements in genetic testing technologies.

Market Size & Forecast

2024 Market Size 1495.68 (USD Million)
2035 Market Size 3793.16 (USD Million)

Major Players

Invitae (US), Myriad Genetics (US), Fulgent Genetics (US), Natera (US), GeneDx (US), Ambry Genetics (US), Quest Diagnostics (US), Laboratory Corporation of America (US)

US Carrier Screening Market Trends

The carrier screening market is currently experiencing notable growth, driven by advancements in genetic testing technologies and increasing awareness among healthcare providers and patients. The integration of next-generation sequencing (NGS) has revolutionized the ability to identify genetic disorders, allowing for more comprehensive screening options. As a result, healthcare professionals are increasingly recommending carrier screening as part of routine prenatal care, which may lead to earlier interventions and informed decision-making for prospective parents. Furthermore, the rise in genetic counseling services is enhancing the understanding of carrier screening results, thereby fostering a more informed patient population. In addition, the regulatory landscape surrounding genetic testing is evolving, with agencies emphasizing the importance of accuracy and reliability in testing methods. This shift may encourage more laboratories to adopt standardized practices, ultimately improving the quality of services offered in the carrier screening market. Moreover, the growing emphasis on personalized medicine is likely to further propel the demand for carrier screening, as individuals seek tailored healthcare solutions based on their genetic profiles. Overall, the carrier screening market appears poised for continued expansion, reflecting a broader trend towards proactive health management and genetic awareness.

Technological Advancements in Genetic Testing

Recent innovations in genetic testing technologies, particularly next-generation sequencing, are transforming the carrier screening market. These advancements enable more accurate and comprehensive testing, allowing for the identification of a wider range of genetic disorders. As a result, healthcare providers are increasingly incorporating these technologies into routine screenings, enhancing patient care.

Increased Awareness and Demand for Genetic Counseling

There is a growing recognition of the importance of genetic counseling in the carrier screening market. As more individuals seek information about their genetic risks, the demand for counseling services is rising. This trend is likely to improve patient understanding of screening results and facilitate informed decision-making regarding reproductive options.

Regulatory Changes and Standardization Efforts

The regulatory environment surrounding genetic testing is evolving, with a focus on ensuring the accuracy and reliability of testing methods. These changes may lead to increased standardization across laboratories, enhancing the overall quality of services in the carrier screening market. Such efforts could foster greater trust among healthcare providers and patients alike.

US Carrier Screening Market Drivers

Rising Prevalence of Genetic Disorders

The increasing prevalence of genetic disorders in the US population appears to be a significant driver for the carrier screening market. As more individuals are diagnosed with conditions such as cystic fibrosis and sickle cell disease, the demand for carrier screening tests is likely to rise. According to the CDC, approximately 1 in 25 individuals of Ashkenazi Jewish descent is a carrier for Tay-Sachs disease, highlighting the need for targeted screening. This growing awareness of genetic risks may lead to a greater emphasis on preventive healthcare measures, thereby expanding the carrier screening market. Furthermore, the integration of carrier screening into routine prenatal care could potentially enhance early detection and management of genetic conditions, fostering a more proactive approach to health in the US.

Legislative Support for Genetic Testing

Legislative initiatives aimed at supporting genetic testing and screening are likely to influence the carrier screening market positively. Recent policies in the US have focused on improving access to genetic testing services, particularly for underserved populations. For instance, some states have enacted laws mandating insurance coverage for carrier screening, which may alleviate financial barriers for patients. This legislative support could encourage more individuals to pursue carrier screening, thereby expanding the market. Additionally, public health campaigns promoting the importance of genetic testing may further raise awareness and acceptance among the general population. As these initiatives gain traction, the carrier screening market may experience increased growth and integration into standard healthcare practices.

Growing Acceptance of Genetic Counseling

The rising acceptance of genetic counseling services is emerging as a key driver for the carrier screening market. As more individuals seek guidance on genetic testing options, the role of genetic counselors becomes increasingly vital. These professionals help patients navigate the complexities of genetic information, ensuring that they understand the implications of carrier screening results. The National Society of Genetic Counselors reports a steady increase in the number of certified genetic counselors in the US, which may enhance the accessibility of these services. This trend suggests that as patients become more informed about their genetic health, the demand for carrier screening is likely to grow. Furthermore, the collaboration between healthcare providers and genetic counselors may facilitate a more comprehensive approach to patient care.

Increased Focus on Preventive Healthcare

The growing emphasis on preventive healthcare in the US is likely to bolster the carrier screening market. As healthcare systems shift towards value-based care, there is a heightened focus on early detection and intervention strategies. Carrier screening plays a crucial role in this paradigm by enabling individuals to understand their genetic risks and make informed reproductive choices. The US Preventive Services Task Force has recommended that all couples planning a pregnancy consider carrier screening for certain genetic conditions, which may further encourage uptake. This proactive approach to health management could lead to an increase in the number of individuals seeking carrier screening, thereby expanding the market. The integration of carrier screening into routine healthcare practices may also enhance patient engagement and awareness.

Advancements in Genetic Testing Technologies

Technological innovations in genetic testing methodologies are transforming the landscape of the carrier screening market. The advent of next-generation sequencing (NGS) has significantly improved the accuracy and efficiency of genetic tests, allowing for the simultaneous analysis of multiple genes. This advancement not only reduces the time required for testing but also lowers costs, making carrier screening more accessible to a broader population. As the price of genetic testing continues to decrease, it is projected that the market will experience substantial growth. The ability to provide comprehensive carrier screening panels that can identify a wide array of genetic conditions may further drive demand, as healthcare providers and patients increasingly recognize the value of early genetic insights.

Market Segment Insights

By Test Type: Panel Testing (Largest) vs. Expanded Carrier Screening (Fastest-Growing)

In the US carrier screening market, the market share is predominantly held by panel testing, which is favored for its comprehensive approach to detecting multiple genetic conditions simultaneously. Single gene testing, while still relevant, captures a smaller slice of the market as it only focuses on individual genes. This segmentation reflects varying preferences among healthcare providers and patients, with panel testing being the most sought-after method due to its efficiency and thoroughness. Growth trends indicate a significant rise in expanded carrier screening, which is becoming increasingly popular due to advancements in genetic technologies and heightened awareness among consumers about genetic conditions. Factors such as rising incidences of genetic disorders and the push for personalized medicine are driving this growth. Innovations and enhancements in testing capabilities further support the rapid adoption of expanded carrier screening, positioning it as a vital segment in the evolving landscape.

Panel Testing (Dominant) vs. Single Gene Testing (Emerging)

Panel testing is the dominant force in the US carrier screening market, recognized for its ability to screen for multiple genetic mutations across various conditions in a single test. This multifaceted approach not only enhances diagnostic accuracy but also streamlines the screening process for both patients and healthcare professionals. On the other hand, single gene testing, while categorized as emerging, remains valuable for specific cases where targeted screening is required. Often utilized for known familial conditions, it serves a critical purpose in the overall testing ecosystem, albeit with a narrowed focus compared to the comprehensive nature of panel testing.

By Technology: Next Generation Sequencing (Largest) vs. Polymerase Chain Reaction (Fastest-Growing)

In the US carrier screening market, Next Generation Sequencing (NGS) holds the largest market share among the technological advancements. Its ability to allow simultaneous analysis of numerous genes contributes significantly to its dominance. With an increasing number of laboratories adopting NGS technology, its market share has steadily expanded, marking it as a critical player in the industry. Conversely, Polymerase Chain Reaction (PCR) is identified as the fastest-growing segment. Its rapid and efficient processing capabilities make it preferred for specific applications, especially in situations requiring prompt results. Growth trends in this segment indicate a burgeoning demand driven by advancements in genetic testing and rising awareness regarding genetic disorders. The introduction of more accurate and accessible screening technologies is propelling the market forward. Additionally, governmental funding and initiatives aiming to enhance carrier screening accessibility are boosting the growth of Polymerase Chain Reaction, making it suitable for a wider demographic and ensuring its status as an emerging technology.

Technology: NGS (Dominant) vs. PCR (Emerging)

Next Generation Sequencing (NGS) is a dominant force within the technological landscape of the US carrier screening market, known for its unparalleled gene analysis capabilities and comprehensive data generation. This technology allows for the sequencing of entire genomes, thereby providing important insights into genetic predispositions that can affect health. Its adoption is widespread among genetic testing laboratories, making it a preferred choice for comprehensive carrier screening. In contrast, Polymerase Chain Reaction (PCR) stands as an emerging technology, characterized by its rapid amplification of DNA sequences, which is particularly advantageous in time-sensitive testing scenarios. The ability of PCR to deliver quick results makes it an increasingly popular choice among healthcare providers, catering to an urgent need for genetic testing in various applications.

By Application: Prenatal Screening (Largest) vs. Newborn Screening (Fastest-Growing)

In the US carrier screening market, the application segment is primarily dominated by prenatal screening, which holds the largest share due to increasing awareness about genetic disorders and advancements in testing technology. Newborn screening follows, supported by legislative mandates and growing parental awareness about early detection of genetic conditions. Growth trends in this segment indicate a robust increase in the adoption of advanced screening technologies. Prenatal screening is propelled by enhanced accessibility and public health initiatives. Conversely, newborn screening is recognized as the fastest-growing segment, driven by technological innovations and the need for timely intervention for genetic disorders, reflecting a growing commitment to preventative healthcare.

Prenatal Screening: Dominant vs. Newborn Screening: Emerging

Prenatal screening has established itself as a dominant force in the US carrier screening market, characterized by comprehensive tests that identify genetic risks during pregnancy. This segment benefits significantly from prenatal care practices and innovations that enhance testing accuracy and convenience. In contrast, newborn screening is emerging as a vital aspect of postnatal care. With advancements in testing methodologies and public health initiatives promoting early diagnosis, this segment is expanding rapidly. The technological evolution, coupled with heightened awareness of genetic conditions among new parents, positions newborn screening as a crucial component in safeguarding infants' health, catering to the increasing demand for early intervention and treatment options.

By End User: Hospitals (Largest) vs. Diagnostic Laboratories (Fastest-Growing)

The US carrier screening market exhibits a diverse distribution of end users, with hospitals commanding the largest share. Hospitals leverage advanced technologies and resources to perform carrier screenings, making them the primary choice for patients. In contrast, diagnostic laboratories are emerging rapidly as significant players, driven by increased demand for genetic testing and personalized medicine, positioning them for a larger market presence in the coming years. Growth trends in the end user segment indicate a robust expansion for diagnostic laboratories, which are capitalizing on the rising adoption of genetic screening protocols. Factors contributing to this growth include technological advancements in testing methods, government support for genetic initiatives, and a growing awareness among patients about the advantages of carrier screening. These dynamics create a competitive landscape where hospitals maintain their dominance while laboratories emerge as fast-growing alternatives.

Hospitals: Dominant vs. Diagnostic Laboratories: Emerging

Hospitals play a pivotal role in the US carrier screening market as they possess the infrastructure to conduct comprehensive genetic tests, providing a wide range of services under one roof. Their established relationships with patients and ability to integrate screenings into prenatal care enhance their market position. In contrast, diagnostic laboratories are considered emerging players, leveraging innovations in high-throughput screening and bioinformatics. They offer specialized services that cater to the growing demand for personalized genetic information among individuals. The focus of laboratories on efficiency and cutting-edge technology allows them to attract an increasing number of clients, posing a significant challenge to the traditional dominance of hospitals in the market.

Get more detailed insights about US Carrier Screening Market

Key Players and Competitive Insights

The carrier screening market is characterized by a dynamic competitive landscape, driven by advancements in genetic testing technologies and an increasing awareness of genetic disorders among prospective parents. Key players such as Invitae (US), Myriad Genetics (US), and Natera (US) are strategically positioned to leverage innovation and partnerships to enhance their service offerings. Invitae (US) focuses on expanding its genetic testing portfolio through acquisitions and collaborations, while Myriad Genetics (US) emphasizes the integration of artificial intelligence (AI) in its testing processes to improve accuracy and efficiency. Natera (US) is also notable for its commitment to digital transformation, utilizing advanced data analytics to refine its carrier screening solutions, thereby shaping a competitive environment that prioritizes technological advancement and customer-centric services.

In terms of business tactics, companies are increasingly localizing manufacturing and optimizing supply chains to enhance operational efficiency. The market appears moderately fragmented, with several players vying for market share, yet the collective influence of major companies like Quest Diagnostics (US) and Laboratory Corporation of America (US) contributes to a more concentrated competitive structure. These companies are not only expanding their testing capabilities but also enhancing their distribution networks to ensure broader access to carrier screening services.

In October 2025, Invitae (US) announced a strategic partnership with a leading healthcare provider to integrate its genetic testing services into routine prenatal care. This collaboration is expected to streamline access to carrier screening for expectant parents, thereby potentially increasing the adoption of genetic testing in clinical settings. The strategic importance of this partnership lies in its ability to position Invitae (US) as a frontrunner in the prenatal genetic testing space, enhancing its market presence and customer engagement.

In September 2025, Myriad Genetics (US) launched a new AI-driven platform designed to enhance the accuracy of its carrier screening tests. This innovative approach not only improves the reliability of test results but also reduces turnaround times, which is crucial in a market where timely information is paramount for decision-making. The introduction of this platform signifies Myriad's commitment to leveraging technology to differentiate its offerings in a competitive landscape.

In August 2025, Natera (US) expanded its carrier screening services by introducing a comprehensive panel that covers a broader range of genetic conditions. This expansion is indicative of Natera's strategy to cater to a growing demand for more inclusive genetic testing options. By broadening its service offerings, Natera (US) aims to capture a larger share of the market, appealing to a diverse customer base seeking thorough genetic insights.

As of November 2025, the carrier screening market is witnessing trends that emphasize digitalization, sustainability, and the integration of AI technologies. Strategic alliances among key players are increasingly shaping the competitive landscape, fostering innovation and enhancing service delivery. Looking ahead, it appears that competitive differentiation will evolve from traditional price-based competition to a focus on technological innovation, reliability in supply chains, and the ability to provide comprehensive, accurate genetic testing solutions.

Key Companies in the US Carrier Screening Market market include

Industry Developments

The US Carrier Screening Market is currently experiencing significant developments and growth, largely driven by advancements in genetic testing technologies and rising consumer awareness. Recent activities include LabCorp's continued expansion of its genetic testing services, as they emphasize personalized medicine.

Myriad Genetics has also enhanced its portfolio, focusing on hereditary cancer testing alongside carrier screening, which reinforces their commitment to comprehensive patient care. Moreover, in September 2023, Fulgent Genetics announced an acquisition of a specialty laboratory specializing in reproductive health to broaden its carrier screening offerings. The merger activity signals a trend towards consolidation, aiming to leverage complementary technologies and improve market positioning.

Additionally, Quest Diagnostics has increased its investments in digital health solutions, enhancing access to carrier screening tests for patients. Overall, the market is witnessing a market valuation growth in companies like Invitae and Color Genomics due to increased demand for genetic insights and preventative healthcare. In the past two years, noteworthy developments have included the introduction of expanded carrier screening panels, reflecting an ongoing trend towards more inclusive testing methodologies.

Future Outlook

US Carrier Screening Market Future Outlook

The Carrier Screening Market is projected to grow at 8.83% CAGR from 2024 to 2035, driven by technological advancements, increasing awareness, and rising demand for personalized medicine.

New opportunities lie in:

  • Development of AI-driven genetic analysis platforms
  • Expansion of telehealth services for remote screening
  • Partnerships with healthcare providers for integrated testing solutions

By 2035, the carrier screening market is expected to achieve substantial growth and innovation.

Market Segmentation

US Carrier Screening Market End User Outlook

  • Hospitals
  • Diagnostic Laboratories
  • Research Institutions

US Carrier Screening Market Test Type Outlook

  • Single Gene Testing
  • Panel Testing
  • Expanded Carrier Screening

US Carrier Screening Market Technology Outlook

  • Next Generation Sequencing
  • Polymerase Chain Reaction
  • Sanger Sequencing

US Carrier Screening Market Application Outlook

  • Prenatal Screening
  • Preconception Screening
  • Newborn Screening

Report Scope

MARKET SIZE 2024 1495.68(USD Million)
MARKET SIZE 2025 1627.74(USD Million)
MARKET SIZE 2035 3793.16(USD Million)
COMPOUND ANNUAL GROWTH RATE (CAGR) 8.83% (2024 - 2035)
REPORT COVERAGE Revenue Forecast, Competitive Landscape, Growth Factors, and Trends
BASE YEAR 2024
Market Forecast Period 2025 - 2035
Historical Data 2019 - 2024
Market Forecast Units USD Million
Key Companies Profiled Invitae (US), Myriad Genetics (US), Fulgent Genetics (US), Natera (US), GeneDx (US), Ambry Genetics (US), Quest Diagnostics (US), Laboratory Corporation of America (US)
Segments Covered Test Type, Technology, Application, End User
Key Market Opportunities Advancements in genomic technologies enhance accuracy and accessibility in the carrier screening market.
Key Market Dynamics Technological advancements and regulatory changes drive growth in the carrier screening market, enhancing consumer access and awareness.
Countries Covered US

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FAQs

What is the expected market size of the US Carrier Screening Market in 2024?

The US Carrier Screening Market is expected to be valued at 1.49 USD Billion in 2024.

What will be the projected market size for the US Carrier Screening Market by 2035?

By 2035, the US Carrier Screening Market is projected to reach a value of 3.79 USD Billion.

What is the expected Compound Annual Growth Rate (CAGR) for the US Carrier Screening Market from 2025 to 2035?

The expected CAGR for the US Carrier Screening Market from 2025 to 2035 is 8.84%.

Which segments of testing are included in the US Carrier Screening Market?

The market includes Single Gene Testing, Panel Testing, and Expanded Carrier Screening.

How much is the Single Gene Testing segment valued at in 2024?

The Single Gene Testing segment is valued at 0.45 USD Billion in 2024.

What will be the value of the Panel Testing segment by 2035?

The Panel Testing segment is projected to be valued at 1.0 USD Billion by 2035.

What is the market value of Expanded Carrier Screening in 2024?

Expanded Carrier Screening is valued at 0.64 USD Billion in 2024.

What are the key players in the US Carrier Screening Market?

Key players in the market include LabCorp, Myriad Genetics, Invitae, and Quest Diagnostics among others.

What opportunities are driving the growth of the US Carrier Screening Market?

Increasing awareness about genetic disorders and advancements in technology are driving growth opportunities.

Are there any challenges facing the US Carrier Screening Market?

Regulatory hurdles and the complexity of genetic testing can pose challenges to market growth.

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