Genetic Testing

Carrier Screening

We all carry genetic changes that we may not know about. These usually do not affect our own health. However, if you and your partner carry the same condition, there may be a chance of passing it on to a child. 

Who is Carrier
Screening for?

Carrier screening is a genetic test that checks whether you are a carrier of certain inherited conditions. It focuses on autosomal recessive and X-linked conditions. Autosomal recessive conditions occur when both parents carry the same genetic change. X-linked conditions are typically carried by females and can be passed on to male children.

Around 1–3% of couples are at risk of having a child with one of these inherited conditions. This testing is usually considered before or early in pregnancy and can provide helpful information when planning a family. 

Carrier screening may be right for you if you are:

Planning a pregnancy and want to learn more about risks to future children

Currently pregnant* and want to learn more about the health of your baby

Have a family history of a genetic condition**

Looking for reassurance....

Come from an ethnic group where carrying certain genetic conditions is more common Eg. Ashkenazi Jewish (Taysachs disease) African (Sickle cell disease)

*Carrier screening pursued in pregnancy needs to take place as early as possible (ie. before 15 weeks).

**If you have a family history of a genetic condition, our genetic counsellors will assess if carrier screening is appropriate or if other testing needs to be considered.

Pricing

Consultation (30 minutes):

For couples attending together, a joint consultation is available at £80

If individuals attend separately, the consultation fee is £80 per person

£80

Genetic Testing

Fulgent Reproductive Carrier Screening (single)

Screening of 700+ genes associated with inherited conditions

£655

Fulgent Reproductive Carrier Screening (Couple):

Screening of 700+ genes associated with inherited conditions

£1,195

Molmart Exome Based Reproductive Carrier Screening (Couple)*:

Screening of 2000+ genes associated with inherited conditions.

£1,600+

*Pricing may vary depending on your testing needs

The cost of your consultation will be applied towards the total cost of testing should you choose to proceed.

How Does It Work?

Our process is simple, supportive, and tailored to you. From your initial consultation through to results, we guide you every step of the way.

Book your consultation

Choose a suitable time and complete a short clinical intake and consent form

Genetic Counselling Session

A qualified genetic counsellor will review your personal and family history and discuss your situation in detail. If appropriate, testing options will be explained, including benefits, limitations, and possible outcomes. All counselling sessions will be followed up with a detail summary letter.

Genetic Testing

Genetic testing will be arranged, as appropriate, after providing informed consent.

Results and follow-up

Your genetic results will be reviewed by a qualified genetic counsellor. These will be delivered to you as agreed in the counselling session. If necessary, a follow-up call to discuss results in more detail can be arranged.

Timeframes

Consultations are typically available within a few days
If testing is undertaken, results are usually available within 4 to 6 weeks

What’s Included

How this can help you

Understand whether you carry specific genetic conditions
Make informed decisions about family planning
Identify any further steps or support that may be appropriate

Our Partner Laboratories

Ready to Book your Carrier Screening?

Book your consultation to explore whether carrier screening is right for you