Carrier screening
This is a comprehensive genetic test that determines whether a person is a carrier of mutations that can be passed on to offspring and cause severe inherited diseases.
Carrier screening for hereditary diseases
What is Carrier screening?
Carrier screening is a genetic test that helps determine whether a person carries mutations associated with inherited diseases. Even if a person is healthy and has no symptoms, they may still be a carrier of a pathogenic variant that can be passed on to their children.
According to studies, each person is, on average, a carrier of 2–3 pathogenic gene variants. Over 80% of children with genetic diseases are born into families with no known history of such conditions.
Carrier screening can be performed before planning a pregnancy or during early pregnancy (up to the 14th week). If both partners are found to be carriers, it is possible to more accurately assess the risk of having an affected child.
Most people do not know they are carriers of a genetic condition until they have a child with that condition. Genscreen carrier screening detects over 10,000 variants associated with 170+ genetic disorders and offers one of the most comprehensive, accurate, and affordable pre-pregnancy screening tests on the market.
How to take the test
You can take the test at our collection point at:
Tashkent, 1st Rakatboshi passage, 17
Blood collection takes no more than 10 minutes. Results are available online or in print.
Carrier screening in the Genscreen Laboratory
International experience
Experts with years of practice in genetics, laboratory diagnostics and bioinformatics.
Confidentiality guarantee
We strictly follow the privacy policy: information is not shared with third parties without consent.
Personal consultation
Online consultation is available to explain results after the study.
Reliability and control
Every research stage is under strict supervision and multiple checks.
Technological leadership
Modern equipment and international diagnostic standards.
Transparent pricing
Clear costs without hidden fees, with the option to choose the most suitable test.