Actionable Genetic Reports for Practicing Healthcare Professionals
$79.00 / file

Healthcare Pro

Genetic analysis and genetic reports designed for healthcare providers


This app can analyze genetic data from any laboratory or company. 

  • The sample report below is from an individual's whole genome sequencing data.
  • This app is powered by's Universal Compatibility technology, which allows the app to be able to analyze genetic data from whole genome sequencing (WGS), exome sequencing and arrays including testing from Illumina, Affymetrix, LabCorp, Quest, Invitae, HLI, 23andMe,, Helix, MyHeritage, Living DNA, Vitagene, HomeDNA, National Geographic and any company or laboratory that provides genetic testing services.



$79 per file

Included is the ability to re-analyze your data an unlimited number of times for one year for no additional fee.

A sample Genetic Report appears above.

In addition to the genetic report, the Healthcare Pro app results also include detailed information about the specific genes and genetic variants analyzed as well as the medical references that link the variant to a specific disease, medication reaction or trait. This information is easy to browse and search with some content linking out to additional information.

To add this app to your My Apps page:

  • Log in to your account.
  • If you are already logged in, click the 'Add to Cart' button located under the app icon (top left of this page).
    • This app will be added to your cart.
    • Click the cart icon that appears in the top right header of the page and follow the instructions to checkout.
      • This app includes a free trial. 
        • After completing the checkout process, you can use this app one time for free within the first 24 hours.
    • This app will immediately be added to your My Apps page.

To use this app:

  1. Log in into your account
  2. Click the 'Add to My Apps' button located under the app icon to add the Healthcare Pro app to your account
  3. Click the 'Start app' button
  4. Select the patient's genetic data file
  5. Click Submit
    • The app will analyze the patient's data and generate a genetic report.
    • You'll receive an email notification when the genetic report is ready to view.
      • Most reports are ready within a few minutes.


*Upload your genetic data at the Upload Center. If you don't yet have genetic data, don't worry! You can use one of our fun sample genomes. Just start the app and select a sample genome.

There are several ways to upload or import your patient's genetic data

  • If your patient already has their genetic data, the patient can register for a free account and upload the data into their secure account.
    • The patient can then easily share the data with you, which allows you to use the data with any app.
  • If you ordered the genetic test, you can upload the genetic data into your practice's secure account. You can then choose to share the data and/or the report(s) with your patient.
  • The laboratory that conducts the genetic testing can also upload the patient's data directly into
    • When a lab uploads data, a secure, free account is automatically created for your patient and he or she will receive the password by email or from the lab.
    • The patient's genetic data will also be automatically shared with your practice's account. You or your staff and then use apps to analyze the data.
      • You and your staff will be able to manage all of your patient's genetic data through your practice's account.
      • Your patients will be able to access their data at any time simply by logging into their accounts at
        • Your patients can use apps to turn their data into useful information, share the data and reports with others or simply use their accounts for free, secure storage of their data.

The results have been specially designed to make them easy to:

  • download as a PDF and quickly import into all EMRs and EHRs.
  • print and add to a chart.
  • securely share with your patient and other healthcare professionals.

If you'd prefer additional EMR/EHR integration, please submit a Support Request to discuss a customized solution. is HIPAA and HITECH compliant. 

Additional information about HIPAA and HITECH compliance can provide you or your organization with a HIPAA Business Associate Agreement (BAA).

Additional information about requesting a BAA

What if I don't have genetic data?

You can still use this app. When you sign into the app for the first time you'll have the option to select from a list of sample genetic data if you don't have your own. All of the sample data are from real individuals so the analysis, results and report are real, too.


What types of genetic data can I use with this app?

You can use genetic data from almost any laboratory genetic test. This includes:

  • Whole genome sequencing and exome sequencing
  • Most DNA genotyping microarrays including Illumina Bead Arrays®, Affymetrix Gene Chips® and the Nexus Chip®
  • 23andMe,, Family Tree DNA and The Genographic Project (National Geographic) 

Please note that the ability for this app to analyze each trait, disease and medication reaction will depend upon the amount of genetic data in your genetic data file. If there is not enough genetic data in your file then some traits, diseases or medication reactions may not be able to be fully analyzed or may not be able to be analyzed at all. The results will indicate if this occurs. For example, if there is no genetic data for a specific disease to be analyzed then the result will indicate 'Not enough data to analyze.' This is more likely to occur if your genetic data file is from a company or laboratory that uses DNA microarray technology for their genetic testing, such as and National Geographic.


Do I need to do anything to the file containing my genetic data before it is analyzed by this app?

Good news... the app does everything for you.

All you need to do is either upload or import the file containing your genetic data into your account. Start the app, select the file and the app will handle do everything else.

23andMe data can be uploaded or imported directly from 23andMe (via the Upload Center) while, Family Tree DNA and The Genographic Project data can be obtained from those services and then uploaded to your account at You don't need to do anything to the file you obtain from these services... just upload the file to your secure account at and then you can use it to power most apps.

Both whole and exome sequencing data can be provided unaligned (such as in FASTQ or FASTA formats), aligned but without variant calling (such as BAM or SAM formats) or in VCF, CRAM or AVRO formats.


What about determining sex or reference genome used when the data was created?

Some more good news... the app does this as well. It utilizes an advanced automated approach to determine sex and reference genome (if the file format is downstream of alignment).


The results include a searchable 'Data & Analysis' table that lists all of the data analyzed by this app. What do the question marks and dashes represent in the 'My Genetic Makeup' column of this table?

Two question marks are used when your genetic data file did not contain any data on this specific genetic variant and therefore the data was not tested for and is 'Unknown'. Two question marks are used because each person's DNA contains two copies of that genetic variant so there is one question mark for each copy of the genetic variant in your DNA.
A single question mark will appear when your genetic data file did not contain any data on this specific genetic and DNA commonly only contains a single copy of that genetic variant. 
For example, all variants on the mitochondrial chromosome (Chromosome "M") exist as a single copy because DNA only contains a single copy of the mitochondrial chromosome. This is different from most chromosomes, which appear duplicate (there are two copies of chromosome 1, two copies of chromosome 2, etc.). If the variant is on a chromosome that there is only a single copy of and there is no data on that variant in the data file then only a single question mark will appear.
Two dashes are used if your genetic data file does include information about this specific genetic variant but the data is a 'No Call.' A 'No Call' means the lab that generated the file determined that the variant's test result did not pass quality control. A 'No Call' may also appear when's additional quality control determines a variant's result is not reliable and may provide inaccurate results. has implemented this additional quality control to ensure that only the highest quality genetic data is analyzed by apps.
Two dashes are used instead of question marks because the genetic data file does contain data on that variant but the variant's results are not reliable.
A single dash is used when the variant's results are not reliable (ie the test result for that variant fails quality control) and DNA contains only a single copy of that variant. For example, all variants on the mitochondrial chromosome that are tested for by a genetic test but don't pass quality control have a single dash as the variant's result.

Wellness & Longevity

Clear solutions for better health. This app analyzes dozens of preventable diseases such as heart disease and cancer and empowers the layperson with a straightforward, actionable report focused on to personalized health optimization.


Rare Disease Screen

Analyzes more than 1,200 rare diseases, syndromes conditions and traits. Determines whether a person is a carrier of, or likely affected by, one or more rare diseases.  Useful for comprehensive analysis of genetic data as well as preconception screening (to identify diseases a person may carry and may pass on to their children).

Click here to view the full list of rare diseases, conditions and traits

The genetic analysis and statements that appear in this app have not been evaluated by the United States Food and Drug Administration. The website and all software applications (Apps) that use's website, as well as's open Application Programming Interface (API), are not intended to diagnose, treat, cure, or prevent any disease.