DNA Carrier Test / Family Planning
The DNA Carrier Status/Family Planning Test analyzes whether you are a carrier of 20 inherited genetic conditions – both autosomal recessive and X-linked. This test is especially relevant if you are planning to become pregnant or want to understand potential genetic risks before starting a family. By taking the test, you gain valuable insights to support informed decisions regarding future pregnancy or fertility choices.
The sample is easily collected via a saliva test and sent to our lab for analysis. The price includes return shipping to the lab. Within 6-8 weeks, you’ll receive your detailed results digitally.
Get 5% off on 2 Lab tests, and 10% off on 3 Lab tests or more.
Find Out If You’re a Carrier of Inherited Genetic Conditions
The DNA Carrier Status / Family Planning Test is an advanced genetic screening that identifies whether you carry inherited conditions that could be passed on to your future children – even if you don’t have any symptoms yourself.
Who Is This Test For?
- Couples planning to have children
- Individuals who want to understand their genetic background
- People with a family history of genetic disorders
- Couples undergoing IVF or fertility treatment
The test is suitable regardless of gender and can be done individually or by both partners to allow for a more complete risk assessment.
What Does the Test Measure?
The test analyzes 20 specific genetic conditions that are inherited either autosomal recessively or X-linked. The following conditions are included:
Autosomal Recessive Conditions:
- Alpha-1 Antitrypsin Deficiency (SERPINA1)
- Biotinidase Deficiency (BTD)
- Cystic Fibrosis (CFTR)
- Familial Mediterranean Fever (MEFV)
- GJB2-related Nonsyndromic Hearing Loss
- Mucolipidosis Type IV (MCOLN1)
- Neuronal Ceroid Lipofuscinosis Type 2 (CLN2)
- Neuronal Ceroid Lipofuscinosis Type 6 (CLN6)
- Neuronal Ceroid Lipofuscinosis Type 8 (CLN8)
- Niemann-Pick Disease, Type A-B (SMPD1)
- Phenylketonuria (PAH)
- Tay-Sachs Disease (HEXA)
- Zellweger Spectrum Disorder (PEX1)
X-linked Conditions:
- Adrenoleukodystrophy (ABCD1)
- Duchenne/Becker Muscular Dystrophy (DMD)
- Fabry Disease (GLA)
- GJB1-related X-linked Charcot-Marie-Tooth Disease
- Hemophilia A (F8)
- Hemophilia B (F9)
- Ornithine Transcarbamylase Deficiency (OTC)
How the Test Works
The DNA Carrier Status test is performed using a simple saliva sample collected at home. The process is straightforward:
- Order the Test: Receive your DNA Carrier Status test kit delivered directly to your home.
- Collect Your Sample: Follow the easy-to-use instructions to collect your saliva sample.
- Send it Back: Use the prepaid return envelope to send your sample to our laboratory.
- Receive Your Results: Within 6-8 weeks, you will get a detailed digital report outlining your methylation pathways along with personalized recommendations.
Sample & Data Privacy
Your DNA and sample material are destroyed after analysis. The sample is linked only to your unique test ID, ensuring complete anonymity. The laboratory does not have access to your identity, and we do not share results with third parties. You also have the option to delete your test results after receiving them.
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The home test was straightforward with easy to follow instructions. The test result was detailed and clear in its presentation. Also had the opportunity to ask questions about the test result.
Richard
We looked at a lot of companies offering the same services but made the decision to go forward with get tested because the labs are based here in the UK. The process has been very straight forward.
Natasha
There are other providers out there, I have tried 3. Gettested was the fastest and the customer service was the best. I even received my test on the day of purchase delivered by a motorbike courier.
Alan
Absolutely perfect, results came after few days and finally after a lots of times visited GP, we finally know why my son has eczema - he is allergy to carrot. Thanks a lot.
E
I found them to be professional and not too long a wait for results. Helpful with any after questions. Will be using them again if need be. I highly recommend them.
Eileen