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Prenatal genetic test checking fetus for inherited cystic fibrosis gene mutations

Cystic Fibrosis DNA Test for Fetus During Pregnancy

Cystic Fibrosis DNA Analysis, Fetus

  • Screen fetus for cystic fibrosis genes
  • Detect inherited mutations from both parents
  • Assess your baby's health outlook
$1591
First results as soon as overnight*

All results normal? Get your money back. First-time customers only. File a support ticket titled “Money Back Guarantee” with your order number within 15 days of receiving your results. STD, Sickle Cell, and gift orders aren’t eligible. Full terms apply. guarantee
No questions asked refunds
LegitScript certified

Prescription & all lab fees included

Go directly to the lab, no extra fees

Doctor's guidance included

Easy to understand results

Fast & convenient

Lab visit as quick as 10 mins in & out

Prescription & all lab fees included

Go directly to the lab, no extra fees

Doctor's guidance included

Easy to understand results

Fast & convenient

Lab visit as quick as 10 mins in & out

All results normal? Get your money back. First-time customers only. File a support ticket titled “Money Back Guarantee” with your order number within 15 days of receiving your results. STD, Sickle Cell, and gift orders aren’t eligible. Full terms apply. guarantee
No questions asked refunds
LegitScript certified

What's this test for?

This test is ideal if you're pregnant and you or the baby's other parent are known or suspected carriers of a cystic fibrosis gene mutation. It checks whether the fetus has inherited the CF-causing mutations from both parents, which is important for understanding your baby's health outlook. Many parents choose this test after carrier screening shows an increased risk, so they can plan next steps early in the pregnancy.

What's included in this test?

This test analyzes the fetal DNA sample for the most common mutations in the CFTR gene, the gene responsible for cystic fibrosis. Testing for a defined panel of known mutations lets you see whether the baby inherited a CF-causing change from each parent, since cystic fibrosis only occurs when a mutation is inherited from both sides.

What happens after I get my results?

Your results will show up securely in your account, with a clear explanation of what a positive or negative finding means for the mutations tested. If the fetus is found to carry two CF mutations, the report will explain what that means and outline options for further evaluation; if no mutations are found in the panel tested, that will also be clearly explained. You can download the standard lab report from your account at any time, and because this is a one-time prenatal test, there's no ongoing trend to track, but you can keep the report on file for your pregnancy records.

When will I get my results?
Results are typically ready within about 7 days of your sample being received at the lab. This timeframe allows for careful genetic analysis of the fetal sample. You'll be notified as soon as your results are posted to your secure account.
Who should consider this test?
This test is a good fit for expecting parents who already know they are CF mutation carriers, or whose carrier screening results raised concern. It's also useful for families with a history of cystic fibrosis, or when one parent has already tested positive as a carrier and the other parent's status is unknown or positive too. Speaking with a genetic counseling resource beforehand can help you decide if this test makes sense for your situation.
What symptoms indicate I may need this test?
Since cystic fibrosis is a genetic condition present from birth, this isn't about symptoms you or the fetus are having now — it's about known carrier status. If prior carrier screening showed you or your partner carry a CF mutation, that's the main signal to consider this test during pregnancy. A family history of cystic fibrosis is another common reason parents pursue this testing.
What is cystic fibrosis and why does it matter?
Cystic fibrosis is an inherited condition that causes thick, sticky mucus to build up in the lungs and digestive system, leading to breathing problems and difficulty absorbing nutrients. It only develops when a baby inherits one mutated copy of the CFTR gene from each parent. Knowing whether your baby has inherited these mutations helps you understand what to expect and plan appropriate care after birth.
What does a positive result mean for the fetus?
A positive result means the fetus has inherited CF-causing mutations detected by this panel, which would mean the baby will likely have cystic fibrosis. This information lets you prepare in advance, such as connecting with a pediatric care team experienced in CF and learning about nutrition, respiratory therapy, and other management approaches used from infancy onward. Early knowledge gives you time to plan and reduce stress after delivery.
What causes cystic fibrosis mutations to be passed to a baby?
Cystic fibrosis happens when a baby inherits one mutated CFTR gene copy from each parent — it's not caused by anything either parent did during pregnancy. If both parents are carriers, there's a 1 in 4 chance with each pregnancy that the baby will have CF, a 1 in 2 chance the baby will be a carrier like the parents, and a 1 in 4 chance the baby will have no mutation at all. This is simply how recessive genetic traits are passed down.
What should I do if my results show a mutation?
If the fetus tests positive for CF mutations, it can help to research support groups and CF specialty care centers so you're prepared for delivery and newborn care. Learning about newborn CF care basics, like nutritional supplements and airway clearance techniques, ahead of time can ease the transition. Genetic counseling resources can also help you understand inheritance patterns for future pregnancies.
How’s this work?
Getting your blood test with us is easy, private & backed by the power of science.

Long story short:
  1. In the test options, use the filters or search box to narrow your choices and find the test you want.
  2. If you need a hand navigating through options, text our super friendly support team at 754-799-7833, and we'll provide tailored suggestions to help you find the ideal test.
  3. Once your order is placed, we’ll create your doctor’s lab order remotely, without any need for you to make a trip to a doctor in person or to talk to the doctor. Expect to receive your doctor’s lab order right in your inbox. It will also be in your patient portal if you need to find it later. We’ll also include instructions regarding fasting and other requirements for your test. Your patient portal will be auto-created hassle-free during checkout.
  4. If this is your first time ordering, you'll be prompted to create a password for instant login access to your patient portal. It's a quick way to conveniently access your orders and results whenever you want.
  5. When you’re ready, visit one of our 4,000 locations. Just bring your ID – no printing or faxing of your lab order is needed, as your order and details will already be in the lab system.
  6. Note that most lab locations don’t accept walk-ins, so it’s best to book an appointment in advance. Don’t worry – we’ll provide detailed instructions along the way.
  7. You’ll get your results via email & SMS and dive into understanding your body better. Yup, that easy!
  8. If you have any questions, please text us at 754-799-7833 or email [email protected] and we'll gladly help you.
How do I know which test to get?
In the test options, find the test you want. If you’re not sure which test to get, we can lend a hand in finding the right option.

Just text or call us at 754-799-7833, email us at [email protected], and we'll gladly help you. We've got your back and reply quickly.
Is it possible to make changes to my lab order if I made a mistake with the name, date of birth, or any other details?
Absolutely! We totally understand that errors can happen. No worries, we're here to help you.

Just reach out to us via text at 754-799-7833 or shoot us an email at [email protected]. Remember to include your order number and let us know the correct information you’d like to update. Our awesome team will jump right in and make sure everything is sorted out and accurate for you.

There are no changes necessary if your address is wrong on the requisition though. We don’t mail anything out.

Our lab requires an address to be listed to generate an order.
Do you accept health insurance?
Only HSA & FSA is accepted.

Our services are strictly self-pay and cannot be submitted to your health insurance provider except for Health Savings Accounts or Flexible Savings Accounts.

This policy applies to all insurance companies, including federal health insurance programs like Medicare.

If you have any questions, please text us at 754-799-7833 or email [email protected].
Can I cancel my order?
Yes.

We get it – sometimes your needs change.

As long as your samples haven’t been collected yet, we’re happy to help you cancel your order.

If you have any further questions, please text us at 754-799-7833 or email [email protected].

You can read more about our cancellation policy here.
How can I find a lab location near me?
During the ordering process, you’ll be able to select a specific lab near you, with no strings attached! You can switch it up later easily and visit any of our authorized locations as long as it’s the same lab company you selected your test for (Quest Diagnostics or Labcorp).

Before you proceed with your order, feel free to browse through all our lab locations here. This will give you the peace of mind of knowing that there's a lab nearby your home, office or your favorite gym.

If you have any questions, please text us at 754-799-7833 or email [email protected] and we'll gladly help you.

Here’s why 1,000,000+ customers chose us for affordable hassle-free private blood testing.

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Demo results
Cystic Fibrosis Mutation Analysis (Fetal DNA) Negative
Demo results
Negative (No Mutations Detected) Positive (Mutations Detected)
Negative

What this means

A negative result means the fetal DNA did not show the common cystic fibrosis mutations tested in this panel. This significantly lowers the chance the baby has cystic fibrosis, though it cannot rule out rare mutations not included in the standard panel. A positive result would mean the fetus inherited mutations from both parents and is expected to have cystic fibrosis.

* Regular blood test results (e.g., CBC) typically start arriving the next business day after sample collection. More advanced tests may take longer due to complexity.
Here’s how easy it is to get blood work done on your terms
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Order your test Save a trip to the doctor. Your results will come with clear, friendly explanations. Takes 2 minutes
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Book an appointment Visit any of our 4,000 nearby lab locations to have your samples collected. Book or walk-in
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Get results Receive a clear, easy-to-digest health report by email & SMS within a few business days. Get answers, fast

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Cystic Fibrosis DNA Test for Fetus During Pregnancy

  • Screen fetus for cystic fibrosis genes
  • Detect inherited mutations from both parents
  • Assess your baby's health outlook
$1591
Still got questions? Text our super-cool support team at 754-799-7833 to get help finding your ideal checkup.
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For informational purposes only. Not medical advice.