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What is the cost of genetic testing, and how long does it take to get the results?
URL of this page: https://medlineplus.gov/genetics/understanding/testing/costresults/

What is the cost of genetic testing, and how long does it take to get the results?

The cost of genetic testing can range from under $100 to more than $2,000, depending on the nature and complexity of the test. The cost increases if more than one test is necessary or if multiple family members must be tested to obtain a meaningful result. For newborn screening, costs vary by state. Some states cover part of the total cost, but most charge a fee of $30 to $150 per infant.

From the date that a sample is taken, it may take a few days to weeks to receive the test results. Results for prenatal testing are usually available more quickly because time is an important consideration in making decisions about a pregnancy. The doctor or genetic counselor who orders a particular test can provide specific information about the cost and time frame associated with that test.

For more information about the logistics of genetic testing:

The National Human Genome Research Institute discusses the coverage and reimbursement of genetic tests.From the National Institutes of Health

Topics in the Genetic Testing chapter

  • What is genetic testing?
  • What are the different types of genetic tests?
  • What are the uses of genetic testing?
  • How is genetic testing done?
  • What is informed consent?
  • How can I be sure a genetic test is valid and useful?
  • What do the results of genetic tests mean?
  • What is the cost of genetic testing, and how long does it take to get the results?
  • Will health insurance cover the costs of genetic testing?
  • What are the benefits of genetic testing?
  • What are the risks and limitations of genetic testing?
  • What is genetic discrimination?
  • Can genes be patented?
  • How are genetic screening tests different from genetic diagnostic tests?
  • How does genetic testing in a research setting differ from clinical genetic testing?
  • What are whole exome sequencing and whole genome sequencing?
  • What are secondary findings from genetic testing?
  • What is noninvasive prenatal testing (NIPT) and what disorders can it screen for?
  • What is circulating tumor DNA and how is it used to diagnose and manage cancer?

Other chapters in Help Me Understand Genetics

The information on this site should not be used as a substitute for professional medical care or advice. Contact a health care provider if you have questions about your health.

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