Identify Genetic Predispositions and Store Your Own Cells

GoodCell's genetic test identifies predispositions to 41 inherited diseases including breast, ovarian and colon cancer as well as cardiovascular disease. When you use an FSA/HSA you receive complementary Personal Biobanking - the storage of your healthiest cells to enable future therapies - all with one simple blood draw. 

Genetic Testing

Personal Biobanking

The GoodCell Advantage

Genetic Testing for 41 Diseases

Identify your inherited risk for 41 diseases such as breast cancer and cardiomyopathy and track any genetic changes year after year. Unlike other genetic tests, GoodCell’s genetic test is medically actionable—which lets you take advantage of medically recommended steps to prevent or lower your risks—and is clinically valid—which means your doctor trusts its results and does not need to request another. 

Complimentary Cell Storage

Preserve your healthiest cells now to protect your future wellbeing. Your personal biobank with GoodCell—a complimentary service with your genetic test—is a secure repository that preserves and stores cells extracted from your blood for future cell-based treatments called cell therapies. By storing them now, you can ensure you have the best chance of participating in these potentially life-saving treatments later.  


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The GoodCell General Health Panel is a curated set of tests that evaluates multiple physiological systems.  

The four tests are as follows: 

  1. Lipid test – measures typical markers of atherosclerosis to assess risk for heart attack, stroke and chronic kidney disease
  2. Vitamin D test – assesses your risk of rickets and osteoporosis, along with the hormonal effects of vitamin D on immunity, body weight, mental health and cancer risk
  3. Hemoglobin A1c test – provides snapshot of blood sugar control over the past three months to screen for undiagnosed prediabetes and diabetes
  4. High-sensitivity C-reactive protein test (hs-CRP) – identifies your levels of a critical plasma marker for low-grade inflammation that contributes to body fat regulation, heart disease and the body’s response to stressors (like infections) 

How to Schedule a Blood Draw

Our national partner for blood draws is Quest Diagnostics. You can find the  Quest Patient Service Centerthat is the most convenient for you or call Quest at: 1-888-277-8772. When you have selected a Patient Service Center and are ready to schedule an appointment, Quest will ask you a few questions:
  1. Who is sending you for testing? Choose “Medical Professional.”
  2. What testing do you need? Choose “Other.”
  3. You may be asked to enter insurance information. This is only required if you reside in  New York, New Jersey or Rhode Island.If you reside in any other state, you can reply “No” to this question.
  4. You will also be asked to provide information to confirm your order and for a method of contact.
On the day of your scheduled blood collection, bring your GoodCell Kit and all documents received with the Kit to your appointment at the Quest Patient Service Center. If we can be of any assistance in helping you to schedule your blood collection or locating a Quest Patient Service Center, please let us know by emailing us at [email protected] or calling us at 800-772-0593.

Tests inherited predisposition to 31 diseases across 59 genes, including:

  1. Arrhythmogenic Right Ventricular Cardiomyopathy
  2. Brugada Syndrome
  3. Catecholaminergic Polymorphic Ventricular Tachycardia
  4. Familial Dilated Cardiomyopathy (FDCM)
  5. Ehlers-Danlos Syndrome, vascular type
  6. Familial Adenomatous Polyposis (FAP)
  7. Familial Hypercholesterolemia
  8. Familial medullary thyroid cancer (FMTC)
  9. Hereditary Breast and Ovarian Cancer
  10. Hereditary paraganglioma-pheochromocytoma syndrome (PGL/PCC)
  11. Familial Hypertrophic Cardiomyopathy
  12. Juvenile Polyposis Syndrome
  13. Li-Fraumeni Syndrome
  14. Loeys-Dietz Syndrome
  15. Lynch Syndrome
  16. Malignant Hyperthermia Susceptibility
  17. Marfan Syndrome
  18. Multiple Endocrine Neoplasia type 1 (MEN1)
  19. Multiple Endocrine Neoplasia type 2 (MEN2)
  20. MUTYH-associated polyposis (MAP)
  21. Neurofibromatosis type 2 (NF2)
  22. Ornithine transcarbamylase (OTC) deficiency
  23. Peutz-Jeghers syndrome (PJS)
  24. PTEN hamartoma tumor syndrome
  25. Retinoblastoma
  26. Romano-Ward Long-QT Syndrome
  27. Thoracic Aortic Aneurysms and/or Dissections (TAAD)
  28. Tuberous Sclerosis Complex (TSC)
  29. Von Hippel-Lindau Syndrome
  30. Wilson disease
  31. WT1-related Wilms tumor