About Ambry Genetics
Ambry Genetics, founded in 1999 by Charles Dunlop, is a genetic testing and diagnostic company. Currently led by Dr. Aaron Elliot, as a part of Konica Minolta Precision Medicine, Ambry has its headquarters in Aliso Viejo, CA, USA. Its labs are CLIA/CAP-certified.
Ambry Genetics Services
Ambry was the first lab to offer BRCA testing and complete gene sequencing services since 2001. With its CLIA/CAP-certified SuperLab, Ambry currently provides the following genetic tests:
- Cardiac conditions
- Neurological conditions
- Hereditary cancer
- Other rare genetic conditions
Ambry offers services only for patients residing in the United States. It does not sell test kits directly to consumers for providing raw DNA data. So, to avail of genetic testing services with Ambry Genetics, you need to contact a healthcare provider first.
Ambry Genetics offers free genetic counseling for people who test positive for a clinically significant mutation associated with cancer. The company also provides other counseling aids and tools on its website to help explain the test results.
Apart from these, Ambry also offers an added-on RNA testing feature, which provides more accurate and actionable results than DNA testing alone. RNA is a molecule similar to DNA but single-stranded. RNA is directly involved in protein production.
Image: DNA to RNA to Protein
Ambry Genetics: Ordering The Tests
Ambry Genetics requires you to take the test through a healthcare provider. After you spell out your needs, they will order the sample collection kit.
Image: Ambry Genetics Ordering Process
You will then need to provide a sample depending on your test type. There are a few ways to submit your DNA sample for genetic testing.
- Your health provider will have a saliva sample collection kit shipped directly to you to provide the sample.
- You may be required to visit a local lab to provide your DNA sample.
- A mobile blood collection kit will be shipped to you to provide the sample.
You can check out the instructions for saliva sample collection here.
Once you collect your sample and send it to Ambry, the lab will run the genetic tests and provide the results to your healthcare provider, who can access it via their login.
What Is The Science Behind The Test?
Ambry uses Clinical Diagnostic sequencing as a discovery tool. It helps improve patient diagnosis and also enables affordable large-scale genetic testing.
Ambry uses quality lab processes, confirmatory testing, and advanced technology to ensure that the results are as informative and accurate as possible.
The team of scientists uses peer-reviewed publications to compile supplementary information for the genetic testing reports.
Overview of the Genetic Test Results
The genetic testing reports may differ from one test to another, but all reports include the following:
The result table displays the following:
- Gene(s) analyzed
- Inheritance mode of the condition
- Mutation/alteration (if present)
- Homozygous or heterozygous state
The interpretation provides a detailed explanation of the results, discussing risk factors and diagnosis. It also includes information on the genes and their variants.
The summary tells you if you have tested positive or negative for the mutation(s) associated with the condition(s) tested.
This section outlines the genetic testing procedure and provides information on the processing of your DNA sample.
Image: Test Results
Reports also contain supplemental information with report references. Additionally, it includes an interspecies comparison with a detailed description of the variations.
Image: Supplemental Information on The Reports
The reports are tailor-made for use by genetic counselors and healthcare providers, including information vital for patient medical care.
Ambry Genetics Pricing
You may qualify for free genetic testing if you have insurance coverage. However, if your insurance does not cover genetic testing, Ambry will consider your financial situation before pricing the test.
Before allowing your healthcare provider to order a kit for you, it is essential to check the details of your health insurance plan. Your health provider will then fill out an insurance pre-verification form to help Ambry estimate the out-of-pocket cost for your genetic testing.
If the test is not covered under your insurance, it may cost around $3000 and extra charges for genetic counseling.
The company provides free genetic testing to patients of select genetic diseases in collaboration with pharmaceutical partners.
Ambry keeps track of user activity and maintains visitor logs to put together anonymous aggregate statistics.
Ambry may collect, store, and use personal information when voluntarily submitted during registration. The company will use this information to contact its users and improve its services.
By accepting Ambry’s privacy terms, you give the company consent to share your information with third-party individuals like genetic counselors, healthcare providers, etc.
What People Say- News & Reviews
- Konica Minolta Inc. acquired Ambry Genetics in a deal worth up to $1 billion in 2017.
- Ambry Genetics ranks among the top players in the US Genetic Testing Market Research Report in 2021.
- Ambry was named Best Company and recognized with five awards by Comparably.
- Ambry Genetics defeated the appeal by competitor Myriad Genetics to restrict genetic testing for ovarian and breast cancer in 2014.
Ambry Genetics Review on Facebook (5/5 - based on 31 reviews)
Ambry Genetics on Google Reviews (3.7/5 - based on 15 reviews)
Summary: Pros, Cons & Verdict
- Testing uses state of the art technology
- Results are reliable due to review by a healthcare provider
- Cost-effective as services may have health insurance coverage
- Reports are accurate and precise
- Provides free counseling for cancer patients
- Access to raw data is unavailable
- Requires users to contact a healthcare provider first
- Does not accept data from other genetic testing providers like AncestryDNA and 23andMe
|Ambry Genetics||Xcode Life|
|DNA kit||Provided||Not provided|
|DNA raw data upload||Not allowed||Allowed|
|DNA data exploration tools||Not available||Available|
|Report prices||$0 – $100 if covered by insurance; very expensive otherwise||$10-$99|
|Report categories||Neurology, Cardiology, Oncology, and Exome & General Genetics||Nutrition, Fitness, Skin, Allergy, Health, Personality, Carrier Status, Breast Cancer, MTHFR, Personalized Medicine, ACMG, Sleep, COVID-19 Genetic Reports|
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