Early Gender Blood test

Can’t wait to find out whether you’re having a little boy or girl? Our Early Baby Gender Blood Test can tell you your baby’s gender from as early as 7 weeks of pregnancy, giving you an exciting glimpse into your pregnancy journey even sooner.

The test is quick, safe and non-invasive, requiring just a small blood sample from mum. It works by looking for tiny traces of your baby’s DNA in your bloodstream. If a Y chromosome is detected, you’re expecting a boy. If no Y chromosome is found, you’re expecting a girl.

With an accuracy of 99.9%, it’s a trusted way to discover your baby’s gender early.


Why choose an Early Baby Gender Blood Test?

Whether you’re excited to start choosing names, planning a gender reveal, decorating the nursery, or you’re simply too excited to wait for your scan, our Early Gender Blood Test gives you the opportunity to find out sooner.

Many parents love knowing early, while others prefer to keep it a surprise until birth—whatever you decide, we’re here to support your journey.


What happens at your appointment?

Your appointment is quick and simple. We will take a small blood sample, which is sent to our specialist laboratory for analysis.

At a glance

💙 99.9% accurate

🩷 Available from just 7 weeks of pregnancy

🩸 Simple, non-invasive blood test

Please note an ultrasound scan is required to confirm gestation.  We will not be able to perform your test without one. If you have had a scan previously please book our bloods only package


The test is analysed by Concepto Diagnostics Ltd., a trusted British healthcare provider with over a decade of experience. Concepto has an in-house UKAS-accredited diagnostics laboratory alongside a state-of-the-art genomics facility.

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NIPT

Understanding Non-Invasive Prenatal Testing (NIPT)

Pregnancy is an exciting time, but it can also bring questions and uncertainty. Non-Invasive Prenatal Testing (NIPT) is an advanced screening test that can provide valuable information about your baby’s chance of having certain genetic conditions, helping you feel more informed and supported throughout your pregnancy.

Unlike invasive procedures, NIPT simply analyses small fragments of your baby’s DNA that are naturally present in your bloodstream. Because the test only requires a blood sample from you, there is no increased risk of miscarriage associated with procedures such as amniocentesis or chorionic villus sampling (CVS). Many parents choose NIPT for the reassurance it can provide during this important stage of pregnancy.

https://www.conceptodiagnostics.co.uk/assets/patient_handbook.pdf

How does NIPT work?

From 10 weeks of pregnancy, a simple blood sample is taken and sent to a specialist laboratory for analysis. Using advanced technology, the test screens for the likelihood of certain chromosomal conditions, including:

  • Down syndrome (Trisomy 21)

  • Edwards syndrome (Trisomy 18)

  • Patau syndrome (Trisomy 13)

NIPT is highly accurate, with detection rates of over 99% for Down syndrome. While it is a screening test rather than a diagnostic test, the results can provide valuable information early in pregnancy, allowing you and your healthcare team to discuss any next steps if needed.

We also offer Advance and Absolute Non invasive prenatal packages.

NIPT Advance detects the following chromosomal anomalies,includes gender reveal (optional, of course).

  • Down Syndrome (Trisomy 21)

  • Edwards Syndrome (Trisomy 18)

  • Patau Syndrome (Trisomy 13)

  • Gender - Male (XY) Female (XX) - (Optional)

  • Sex chromosome anomalies

  • DiGeorge syndrome 2

  • 1p36 microdeletion syndrome

  • Angelman syndrome/Prader-Willi syndrome (15q11-q13 deletion syndrome)

  • Prader-Willi-like syndrome (SIM1 syndrome)

  • Cri-du-chat syndrome (5p deletion syndrome)

  • 4p16.3 deletion syndrome (Wolf-Hirschhorn syndrome)

Our Absolute package includes

NIPT Absolute detects the following chromosomal anomalies, our most comprehensive NIPT test package yet, NIPT Absolute checks for a wide range of chromosomal anomalies along with microdeletions, includes gender reveal (optional, of course).

  • Down Syndrome (Trisomy 21)

  • Edwards Syndrome (Trisomy 18)

  • Patau Syndrome (Trisomy 13)

  • Gender - Male (XY) Female (XX) - (Optional)

  • Sex chromosome anomalies

  • 92 microdeletions

Why choose prenatal NIPT?

Prenatal NIPT offers a safe, reliable and convenient way to learn more about your baby’s health.

Benefits include:

  • A simple, non-invasive blood test with no increased risk of miscarriage.

  • Available from 10 weeks of pregnancy.

  • Highly accurate screening for the most common chromosomal conditions.

  • Fast, confidential results, usually available within a few days.

  • Optional baby gender identification for singleton pregnancies and identical twins.

Whether you’re seeking reassurance or would simply like more information about your pregnancy, NIPT can help you make informed decisions with confidence.

While these tests are generally offered on the NHS only to pregnancies considered to be at higher risk, private testing is available to anyone who wishes to access this screening from 10 weeks onwards.

Supporting you every step of the way

We understand that waiting for test results can feel overwhelming. If your screening result indicates an increased chance of one of the conditions tested, you won’t be left to navigate it alone. Complimentary post-test genetic counselling is included to help you understand your results, answer your questions, and support you in considering any recommended next steps.

The test is analysed by Concepto Diagnostics Ltd., a trusted British healthcare provider with over a decade of experience. Concepto has an in-house UKAS-accredited diagnostics laboratory alongside a state-of-the-art genomics facility.

**Post test counselling is offered by a Fetal Medicine consultant associated with our partner Concepto

For further infotmation please click the following link

https://www.conceptodiagnostics.co.uk/assets/patient_handbook.pdf

 
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