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Genetic carrier screening

Also called: Carrier test, Expanded carrier screening

Carrier screening checks whether you carry a gene change for inherited conditions, like cystic fibrosis, sickle cell disease, or spinal muscular atrophy, that could pass to a child.

SampleBlood or saliva
Fasting?Usually not needed
Results1 to 3 weeks
Good to knowOne result rarely tells the whole story. Your provider looks at your results together with your symptoms, exam, and other tests.

What the test is

It's offered before or early in pregnancy. Carriers are usually healthy.

Why it's done

  • Planning a pregnancy or early pregnancy
  • Family history of a genetic condition

Getting ready and what happens

  • No preparation is needed.

How the test is done

  • A blood draw or saliva sample.

What the results mean

You're a carrier

Your partner may be tested. If both of you carry the same condition, each pregnancy has a 1 in 4 chance of being affected; a genetic counselor can explain options.

Questions to ask your provider

  • What do my results mean for me?
  • Do I need to repeat this test or have other tests?

Risks

A blood draw is very safe. You may have slight pain or a small bruise where the needle went in.

Related conditions

Related tests

Sources

Last updated 2026-11-13.