How Much Does the Harmony Prenatal Test Cost?

Written by: Staff
Last Updated:  August 10, 2018

The Harmony prenatal test utilizes a uniquely targeted DNA analysis system to help screen your unborn child for any chromosomal abnormalities in as early as 10 weeks.

The test, according to the company, can also determine the fetal sex and the number of X and Y sex chromosomes in three steps.

The noninvasive prenatal test (NIPT) test when analyzing the cell-free DNA, will offer a strong indication if the fetus is high at risk of having either trisomy 21 (Down syndrome), trisomy 18 (Edwards syndrome) or trisomy 13 (Patau syndrome).

The test identifies 99 percent, not all, of Down syndrome, 97 percent of fetuses with Edwards syndrome and 92 percent with Patau syndrome.

Akiko Yabuuchi, a Ph.D. in George Daley’... by NIH-NCATS, on Flickr
Akiko Yabuuchi, a Ph.D. in George Daley’…” (CC BY 2.0) by NIH-NCATS

How much does the Harmony prenatal test cost?

Even though the company doesn’t post prices on its website, it appears, from our research, that the average cost can range anywhere from $200 to more than $800 for the test without insurance and if you were to take advantage of the company’s self-pay option.  While some health insurance carriers may cover the procedure or at least a portion, you will have to check your insurance policy to see if this type of testing is eligible.  In most cases, as long as you’re considered high risk and you meet the insurance company’s criteria for being high risk, then there’s a good chance your test will be covered and you will only be responsible for your co-pays/deductible, etc.  Most people, even with insurance, were in the same range mentioned prior when paying out of pocket.

On this forum thread, for example, multiple forum members discussed the prices they paid for their procedure.  According to the responses, the prices ranged anywhere from $200 to more than $800+

Members of this forum thread also discussed the prices they had paid for the Harmony test, with most reporting prices between $200 to $600.

Sonic Genetics, one of the world’s largest medical diagnostics companies, stated the cost of the test, if performed via them, was $425.

How does the test work?

As mentioned, the test works in three steps.  The first step requires a blood sample after the 10-week mark.  This blood sample is then sent off to the Harmony laboratory where it will then be analyzed.  On average, the results can take up to 10 days, and once the analysis has been done, it will be sent to your local health provider.

This non-invasive test will use your blood work to help detect any chromosomal disorders by using its exclusive DANSR™ technology, which, according to the company, focuses solely on the fragments of the baby’s DNA floating in the mom’s blood in tied in connection with FORTE™, an algorithm that is able to distinguish the high- and low-risk results.

The extra costs

Even if the results are positive, it does not mean the fetus is said to have the defects guaranteed.  To be certain, a CVS or amnio will be recommended to confirm the results.  With that being said, there may be extra costs associated with the testing, depending on your circumstances.  For instance, a chorionic villus sampling and amniocentesis may be used if a chromosomal abnormality were suspected via genetic counseling or a blood test such as this.

The company offers additional tests for a fee such as a fetal sex test, Monosomy X test, sex chromosome aneuploidy panel and 22q11.2.

Tips to know

The company does have multiple published medical studies, all of which are posted on their official website found here.  The company claims to be the most broadly studied non-invasive prenatal test (NIPT) for Down syndrome (trisomy 21), Edward syndrome (trisomy 18), and Patau syndrome (trisomy 13).

Don’t be scared when you receive your explanation of benefits and see a high cost.  It’s highly reported that even if the “patient responsibility” is in the high $xxx, most reported the costs, in the end, to be much less than what was quoted via their insurance company’s official paperwork.

This test, as compared to other tests, will deliver clear answers as early as the first trimester with a simple blood draw.  As some screenings are performed much later in the pregnancy and require multiple office visits, the test, using a unique method of targeted DNA analysis, combined with quality controls, is able to achieve a higher than 99 percent accuracy rate.

The test, aside from screening for chromosomal abnormalities, is also able to evaluate the fetal sex and the number of the X and Y sex chromosomes.

How to save money

Ariosa Diagnostics, the developer of the product, does offer a sliding fee schedule for those who do qualify.  A discounted program is also available for those who do pay their bill in full within 30 days.  In a lot of cases, customers were able to call the lab directly and they were willing to haggle on the price.  Payment plans are also available.

Always talk with your insurance company ahead of time to see if they will cover this type of test.  As long as you have a procedure code and/or the exact lab test name, you should be able to get an idea over the phone.  As all insurance company policies are different, there are way too many factors involved to offer a definite answer.

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