The global carrier screening market size is estimated to reach USD 4,045.29 million by 2033, registering a CAGR of 11.95% from 2025 to 2033, according to a new report by Grand View Research, Inc. The increase in technological advancement in carrier screening along with the rising adoption of in vitro fertilization in emerging markets is expected to boost the market growth during the forecast period. The carrier receives the abnormal gene from the parents. Disorders such as sickle cell anemia, cystic fibrosis, Tay-Sachs disease, fragile X syndrome, and SMA can be identified using carrier screening.
Molecular tests are performed to detect the mutation by finding the abnormalities in the DNA. Next-generation sequencing is one of the techniques to perform tests. There is the possibility of the carrier not showing any symptoms and signs of illness. The test is recommended for pregnant women to check whether the baby will have a chance of genetic deformities. It is also advised to the male parent of the child to undergo the carrier screening test. The early-stage disease diagnosis and restraint of these genetic deformities is expected to augment the market growth. The test involves the tissue cells of the cheeks, blood, or saliva samples.
The adoption of carrier screening in the precision medicine market is also increasing. According to the article published in November 2022, by The Medical Journal of Australia, stated that the rapid innovations in genomic medicine along with sequencing technology for genetic code created a lucrative opportunity for genetic carrier screening. For incorporating population screening into precision medicine, a framework such as RE-AIM can be employed to plan research, assess barriers, and evaluates the result. This strategy was employed to assess the population DNA screening in the U.S.
The growing strategic initiatives by hospitals and regulatory bodies to increase the accessibility of carrier screening are expected to support market growth. For instance, in June 2022, NHS announced the expansion of BRCA genetic testing for the Jewish community. Since, 1 in 40 Jews is reported to be the carrier of BRCA, which increases the probability of certain cancers. Similarly, in June 2022, UnitedHealthcare Community proposed to introduce a coverage program for Ashkenazi Jewish Carrier Screening in the U.S.
On the other hand, limited implementation of public health screening, lack of genomic knowledge for reproductive health and primary care, and cost of genomic tests in the emerging market are expected to hamper the market growth. In India, the cost of carrier genetic screening ranges from USD 218 to USD 290. Considering the average purchasing power in the region, the cost is high for the majority of the population.
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By type, the expanded carrier screening segment is projected to establish the significant CAGR over the forecast period. Since increasing product development by the existing players to expand the usage of screening in various fields, such as precision medicine and IVF.
By medical condition, the cystic fibrosis segment accounted for the largest market share of 36.0% in 2024. Owing to the increase in the disease incidence rate and carrier frequency. The product development by the players is likely to support the growth of the segment.
By technology, the DNA sequencing segment held the largest market share of 44.2% in 2024. The adoption of NGS technology for prenatal diagnostics is considered to be the key driver.
By end-user, the laboratory segment is projected to have a majority of the market share in 2024. This is attributed to the presence of well-equipped facilities in developed countries, along with the increasing tests in the rural areas of emerging markets.
North America has strengthened its regional position in the market with 46.95% of the overall market share in 2024. This is attributed to the presence of hospitals and reference labs, along with the existence of key players in the region.
Grand View Research has segmented the global carrier screening market based on medical conditions, type, technology, end-use, and region:
Carrier Screening Medical Conditions Outlook (Revenue, USD Million, 2021 - 2033)
Spinal Muscular Atrophy
Cystic Fibrosis
Tay-Sachs
Gaucher Disease
Sickle Cell Disease
Others
Carrier Screening Type Outlook (Revenue, USD Million, 2021 - 2033)
Expanded Carrier Screening
Targeted Disease Carrier Screening
Carrier Screening Technology Outlook (Revenue, USD Million, 2021 - 2033)
DNA Sequencing
Polymerase Chain Reaction
Microarrays
Other Technologies (MLPA, Genotyping, Enzyme Screening)
Carrier Screening End-use Outlook (Revenue, USD Million, 2021 - 2033)
Hospitals
Laboratories
Physician Offices & Clinics
Other End Users
Carrier Screening Regional Outlook (Revenue, USD Million, 2021 - 2033)
North America
U.S.
Canada
Mexico
Europe
UK
Germany
France
Italy
Spain
Denmark
Sweden
Norway
Asia Pacific
Japan
China
India
Australia
South Korea
Thailand
Latin America
Brazil
Argentina
Middle East & Africa
South Africa
Saudi Arabia
UAE
Kuwait
List of Key Players of Carrier Screening Market
Myriad Genetics, Inc.
BGI Genomics
Illumina, Inc.
Thermo Fisher Scientific, Inc
F. Hoffmann-La Roche Ltd
Laboratory Corporation of America Holdings (LabCorp)
Otogenetics Corporation
MedGenome
GeneTech (ATS Genetech Pvt Ltd)
CENTOGENE GmbH
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