Strategic Forecast for the Carrier Screening Industry: Market Outlook 2025-2034

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Carrier Screening Market Size Growth Forecast: What to Expect by 2025?
In the past few years, the size of the carrier screening market has seen a significant increase. It is projected to expand from a market size of $2.72 billion in 2024 to $3.17 billion in 2025, corresponding to a compound annual growth rate (CAGR) of 16.4%. The surge during the historical period is a result of growing awareness of genetic disorders, increasing maternal age, awareness of family planning and pregnancy, prevention of genetic diseases, public health initiatives and an enhanced concentration on inherited situations.

How Will the Carrier Screening Market Size Evolve and Grow by 2029?
In the coming years, the size of the carrier screening market is anticipated to witness rapid expansion. It is predicted to reach a valuation of $5.76 billion by 2029, growing at a compound annual growth rate (CAGR) of 16.2%. The progress in the prediction period can be linked to advancements in precision medicine, enhanced panel offerings, consumer genomics, and direct-to-consumer testing, emphasis on rare and ultra-rare diseases, support from government and insurance, and the integration of pharmacogenomics. Noteworthy trends for the future include the development of genetic technologies, fusion with prenatal testing, increase in personalized medicine, counseling, and education services, as well as moral and legal considerations.

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What Drivers Are Propelling the Growth of Carrier Screening Market Forward?
The carrier screening market is projected to expand due to the rise in fetal chromosomal abnormalities and genetic disorders. Fetal chromosomal abnormalities denote a fetus with an atypical number of chromosomes or irregular quantity of DNA within a chromosome. Chromosomal abnormalities are detected through prenatal testing to reliably evaluate the risk of a patient carrying a fetus with such a disorder. For example, the World Health Organization, a Swiss-based international health institution, reported in February 2022 that birth defects are responsible for the death of 240,000 newborns within the first 28 days of life annually. Further, birth defects claim the lives of an additional 170,000 children aged between 1 month and 5 years. Additionally, a March 2022 article released by the United Nations Government estimated that Down syndrome impacts 1 in 1,000 to 1 in 1,100 live births globally. This chromosomal disorder is born by between 3,000 and 5,000 children annually. Consequently, the rise in fetal chromosomal abnormalities and genetic disorders is catalyzing the growth of the carrier screening market.

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Which Emerging Trends Are Transforming the Carrier Screening Market in 2025?
Major enterprises involved in the carrier screening industry are centering their efforts on product enhancement, such as the creation of family screening tests, to maintain their market stance. These screening tests are health procedures or tests conducted on people who show no signs of certain diseases or conditions. For instance, Blueprint Genetics, a company based in Finland that excels in genetic testing and diagnostics, brought to the market a new product known as the Screening Tests family in June 2023. The product is tailored for specific purposes including pregnancy, family planning, and thorough health examinations for people without symptoms. The goal is to spot any increased risks, thereby enabling individuals to make educated choices about family planning and their health. Blueprint Genetics is determined to provide actionable insights, allowing proactive decision-making based on available alternatives. The primary focus is on aiding individuals in making knowledgeable decisions about their future health.

What Are the Key Segments in the Carrier Screening Market?
The carrier screening market covered in this report is segmented -

1) By Type: Expanded Carrier Screening, Targeted Disease Carrier Screening
2) By Medical Condition: Pulmonary Conditions, Hematological Conditions, Neurological Conditions, Other Medical Conditions
3) By Technology: DNA Sequencing, Polymerase Chain Reaction, Microarrays, Other Technologies
4) By End User: Hospitals, Reference Laboratories, Physician Offices And Clinics, Other End Users

Subsegments:
1) By Expanded Carrier Screening: Whole Exome Sequencing (WES), Next-Generation Sequencing (NGS) Panels, Comprehensive Carrier Screening Tests
2) By Targeted Disease Carrier Screening: Single Gene Tests, Disease-Specific Panels, Ethnic Or Population-Specific Screening Tests

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Who Are the Key Players Shaping the Carrier Screening Market's Competitive Landscape?
Major companies operating in the carrier screening market are Invitae Corporation, BGI Genomics Co. Ltd., Centogene NV, Eurofins Scientific SE, Fulgent Genetics Inc., Genealogy by Genetics Ltd., Illumina Inc., Laboratory Corporation of America Holdings, Luminex Corporation, MedGenome Inc., Myriad Genetics Inc., Natera Inc., OPKO Health Inc., Otogenetics Corporation, Quest Diagnostics Inc., Sema4 Holdings Corporation, Thermo Fisher Scientific Inc., 23andMe Holding Co., REALM IDx Inc., Associated Regional and University Pathologists Inc., Genedx LLC, Genomic Health Inc., GenPath Consultants And Technologies Private Limited, Good Start Genetics Inc., NIPD Genetics Co. Pvt. Ltd., OraSure Technologies Inc., Pathway Genomics Corp., PerkinElmer Inc., PreventionGenetics LLC, Progenity Inc.

What Geographic Markets Are Powering Growth in the Carrier Screening Market?
North America was the largest region in the carrier screening market in 2024. Asia-Pacific is expected to be the fastest-growing region in the carrier screening market report during the forecast period. The regions covered in the carrier screening market report are Asia-Pacific, Western Europe, Eastern Europe, North America, South America, Middle East, Africa.

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