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Breast Cancer STAT Panel logo

Is the Invitae Breast Cancer STAT Panel the right test for you?

All of us have a 1 in 2 lifetime risk of cancer, but some common cancers – breast, melanoma, pancreatic, prostate and ovarian – are known to occur more frequently in families, passing from one generation to the next.

It’s because certain gene mutations can be inherited – particularly those in BRCA1 and BRCA2 genes – and this test focuses on these, plus another six genes which can indicate additional risk.

The results will enable you and your clinician to plan screening or preventative treatment to minimise your risk and improve overall survival rates.

If you have already been diagnosed with cancer, this test is a rapid analysis that can help you make vital decisions about your treatment – particularly if you are considering surgical options.

Your clinician can explain the specific criteria which would make this the right test for you are considered to be at high risk if you have early-onset or multiple diagnoses of breast cancer, male breast cancer, and/or have a family history of disease.

To get this test you will first need a consultation with your clinician, then you can either:

  • Buy it directly from this website (this cost may be covered by your medical insurance).
  • Access it through your treating hospital/private healthcare provider.

This test is only available to those aged 18 years or above.

Our price £595 (RRP £995) Save £400

Got a box? Enter your serial number in the box below. It is located on the reverse of the kit and consist of 14 numbers.

If you need any assistance, please call +44 (0) 1270 699 021.

Why?Close tab

Helping you make decisions

Understanding whether you have a genetic predisposition to cancer allows you to make informed decisions about monitoring and treatment that can significantly decrease cancer risks and improve overall survival rates.

For example, you could decide at what age to have your first mammogram and breast MRI scan – and how frequently to have them in the future.

If you need to make urgent decisions about treatment – perhaps whether to have a lump removed or a full or partial mastectomy – this test can give you and your clinician the vital knowledge to make an informed decision.

For your family

It’s also important to share the test analysis with your family: because, there could be implications for them too. For example, if a man or woman carries a mutation in BRCA1 (one of the genes tested), each of their parents (mother and father), siblings (brothers and sisters) and children (sons and daughters) have a 50% chance of carrying the same mutation. Knowing if this gene mutation is in the family means everyone can ensure they receive regular monitoring and screening.

You can discuss this with your clinician, or if you would like to talk to one of our experts about the test, call us on +44 (0) 1270 699021.

How?Close tab

What do I need to do?

It’s a simple ‘spit test’ that you can do in your own home – we don’t need a blood sample, all we need is your saliva. You’ll receive a kit in the post with clear instructions on giving your sample together with all the paperwork you need to sign, which you then post back to us.

ProcessClose tab

Buying the test

Step 1: There are two options:

  • Via your treating hospital/private healthcare provider (we have special arrangements with many healthcare providers to enable you to access this test, click here to see the list)
  • By clicking the ‘Buy direct now’ button above (the cost may be covered by your medical insurance – check your policy details)

Step 2: Collection of sample

We will liaise directly with your clinician and organise the collection of your sample and delivery to the laboratory.

Step 3: Analysis and reporting

Your sample will be analysed and a report will be generated, results are provided 2 weeks after your sample is received in the lab. Please allow additional time for delivery to the lab.

Step 4: Results

Your clinician will receive the test report giving a clear indication of whether you are at risk of cancer or if you have already been diagnosed, what steps you – and possibly other members of your family – need to take next.

ResultsClose tab


Your clinician will be able to discuss your results and their implications for you, but as a guide:


A positive result does NOT mean you have cancer, or that you will definitely develop it.

It does means that a mutation, or genetic change, has been identified in a specific gene that increases the chance of your developing certain cancers in your lifetime – and your personal results will provide more detailed information specific to you. Talk to your clinician about creating a screening and management plan for you, and to identify relatives who may also need to be tested.


A negative result means that no mutations or genetic changes associated with an increased risk of the most common hereditary cancers were identified in the genes that were analysed. The result does not eliminate your risk of developing cancer completely as there are other factors, such as lifestyle, or perhaps mutations not detected by current technology or mutations in other genes. Again, talk to your clinician about what the results mean for you.

Variant of uncertain significance

This is where a gene mutation has been found, but at present we do not know if this affects your risk of certain cancers. In this case, your clinician will be able to talk about screening recommendations based on your personal and family medical histories and if new information becomes available, Invitae will update your clinician.

CliniciansClose tab

Is the Invitae Breast Cancer STAT Panel the right test for your patient?

This panel comprises genes for which there are established medical management guidelines. It may be considered for individuals with a personal and/or family history of:

  • breast, ovarian, uterine/endometrial, colon, pancreatic, melanoma, sarcoma, and/or prostate cancer, particularly if early onset (<50 years)
  • male breast cancer
  • breast or ovarian cancer and Ashkenazi Jewish ancestry

There are also some common, general features suggestive of a hereditary cancer syndrome family. These include:

  • cancer diagnosed at an unusually young age
  • different types of cancer that have occurred independently in the same person
  • cancer that has developed in both organs of a set of paired organs (e.g., both kidneys, both breasts)
  • several close blood relatives that have the same type of cancer
  • unusual cases of a specific cancer type (e.g., male breast cancer)

Test Description

The Invitae Breast Cancer STAT Panel includes up to 9 well-established genes that are associated with a significantly increased risk of developing breast cancer. Accelerated turnaround time (TAT) is needed because physicians and patients often want to make surgical and management decisions as quickly as possible. Individuals who are identified with an inherited pathogenic variant have a higher risk of developing another breast cancer and may choose more aggressive surgery and/or different treatment options based on genetic testing results.

All genes on this panel have published medical management guidelines and are associated with defined hereditary cancer syndromes.

This test is appropriate for breast cancer patients with upcoming cancer-related breast surgeries and/or treatment where genetic testing may inform decisions such as lumpectomy versus mastectomy, single versus double mastectomy, or use of other treatments (such as use of PARP inhibitors or other chemotherapy regimens). Identification of a disease-causing variant may also guide testing and management of at-risk relatives. This test is specifically designed for heritable germline mutations and is not appropriate for the detection of somatic mutations in tumour tissue.

ValidationClose tab

This test is provided by:


Frequently asked questions

Do I need a doctor to authorise this test?
Yes, your doctor will need to provide the sample required for this test.
Will my health insurance cover the cost of this test?
Many health insurance plans cover the cost of genetic testing – check with your provider to find out if it is in your policy.
How accurate is the test?
All our partners follow advanced laboratory procedures and ensure quality control to deliver accurate results you can trust.