Search Tests - PreventionGenetics

Menu

Menu
  • Testing

      Test Menu

      • PGnome
      • PGxome
      • Custom Panels
      • Tests by Category
      • Targeted Variants
      • How To Order
      • Prenatal
      • All Tests
      • Tests by Disease

      Partner Programs

      • Sponsored Testing
      • Partnership Information
  • Billing

      Billing Information

      • Billing Policy
      • CPT Codes
      • In-network Health Plans
      • Utilization Management
      • FAQs
      • Forms
  • Resources

      Test Information

      • Sample Reports
      • Test Methods
      • Variant Interpretation
      • Family Testing

      Education

      • Webinars

      Policies

      • Terms & Conditions
      • Privacy Practices & Policies
  • How to Order

      Process

      • Log In / myPrevent
      • Ordering Instructions
      • Ordering Instructions
      • Report Retrieval
      • Turnaround Time
      • Forms
      • Order Kits

      Additional Info

      • Specimens & Shipping
      • Sample Reports
      • FAQs
      • Sending NY Specimens
      • Family Follow-up Testing
  • DNA Banking

      Providers

      • About DNA Banking
      • Order DNA Banking
      • Order Banking Kits
      • Paper Forms
      • Specimen Requirements
      • Post-Mortem DNA Banking
      • Resources
      • FAQs
      • PGDNABank
        For Patients
  • About Us

      PreventionGenetics

      • About PreventionGenetics
      • Senior Staff
      • Quality & Value
      • Publications
      • Licenses and Certificates
      • PGNewsroom
      • Join Our Team
  • Contact Us
  • Forms
    • 0

    • Log In / Sign Up

      myPrevent

  • Menu
HOME | CONTACT US | FORMS |

Log In / Sign Up

myPrevent

|

0

  • Testing

      Test Menu

      • PGnome
      • PGxome
      • Custom Panels
      • Tests by Category
      • Targeted Variants
      • How To Order
      • Prenatal
      • All Tests
      • Tests by Disease

      Partner Programs

      • Sponsored Testing
      • Partnership Information
  • |
  • Billing

      Billing Information

      • Billing Policy
      • CPT Codes
      • In-network Health Plans
      • Utilization Management
      • FAQs
      • Forms
  • |
  • Resources

      Test Information

      • Sample Reports
      • Test Methods
      • Variant Interpretation
      • Family Testing

      Education

      • Webinars

      Policies

      • Terms & Conditions
      • Privacy Practices & Policies
  • |
  • How to Order

      Process

      • Log In / myPrevent
      • Ordering Instructions
      • Ordering Instructions
      • Report Retrieval
      • Turnaround Time
      • Forms
      • Order Kits

      Additional Info

      • Specimens & Shipping
      • Sample Reports
      • FAQs
      • Sending NY Specimens
      • Family Follow-up Testing
  • |
  • DNA Banking

      Providers

      • About DNA Banking
      • Order DNA Banking
      • Order Banking Kits
      • Paper Forms
      • Specimen Requirements
      • Post-Mortem DNA Banking
      • Resources
      • FAQs
      • PGDNABank
        For Patients
  • |
  • About Us

      PreventionGenetics

      • About PreventionGenetics
      • Senior Staff
      • Quality & Value
      • Publications
      • Licenses and Certificates
      • PGNewsroom
      • Join Our Team

Browser Upgrade Recommended. More Info

We have detected that you are using Internet Explorer or Microsoft Edge Legacy. Please consider upgrading your browser to any of the following for the best experience.

  • Google Chrome
  • Firefox
  • Microsoft Edge
  • Safari

Login

Forgot username?

Forgot password?

Don't have an account?

×
  • Test By Category
  • View All Tests
  • View All Panels

FILTERS

ORDER
Test Kits

RESULTS KEY

  • Tests & Panels
  • Categories
  • Newsroom
  • Custom panels
  • Pages & Documents
  • Webinars

Searched: Hereditary Paraganglioma Pheochromocytoma Syndrome Panel

Search Results

  • DNA in a shopping cart Hereditary Xerocytosis Panel
    Test Code
    Method
    Price
    10087
    Sequencing with CNV PGxome
    $890
  • DNA in a shopping cart Hereditary Polyposis Panel
    Test Code
    Method
    Price
    5465
    Sequencing with CNV PG-Select
    $540
  • DNA in a shopping cart Comprehensive Movement Disorders Panel
    Test Code
    Method
    Price
    16004
    Sequencing with CNV PGxome
    $1490
  • DNA in a shopping cart Primary Ciliary Dyskinesia (PCD) via the RSPH4A Gene
    Test Code
    Method
    Price
    747
    Sanger Sequencing
    $690
    8513
    Sequencing with CNV PGxome
    $890
  • DNA in a shopping cart Primary Ciliary Dyskinesia (PCD) via the RSPH9 Gene
    Test Code
    Method
    Price
    748
    Sanger Sequencing
    $540
    9037
    Sequencing with CNV PGxome
    $890
  • DNA in a shopping cart Hereditary Endometrial Cancer Panel
    Test Code
    Method
    Price
    5457
    Sequencing with CNV PG-Select
    $540
  • DNA in a shopping cart Hereditary Ovarian Cancer Panel
    Test Code
    Method
    Price
    5469
    Sequencing with CNV PG-Select
    $749
  • All

    …the APOA1 Gene Test Code Method Price 1403 Sanger Sequencing $580 8867 Sequencing with CNV PGxome $890 Familial Atrial Fibrillation Syndrome Panel Test Code Method Price 10323 Sequencing with CNV PGxome $890 Familial Chylomicronemia Panel Test…

  • All

    …$890 2008 Sanger Sequencing $580 Bardet-Biedl Syndrome (BBS) Panel Test Code Method Price 10349 Sequencing with CNV PGxome $890 Bardet-Biedl Syndrome via the ARL6/BBS3 Gene Test Code Method Price 15145 Sequencing with CNV PG-Select $640…

  • DNA in a shopping cart Neuroblastoma Panel
    Test Code
    Method
    Price
    5057
    Sequencing with CNV PGxome
    $890
  • DNA in a shopping cart Hereditary Hemolytic Anemia Panel
    Test Code
    Method
    Price
    12041
    Sequencing with CNV PGxome
    $890
  • DNA in a shopping cart Hereditary Cystic Kidney Diseases Panel
    Test Code
    Method
    Price
    10619
    Sequencing with CNV PGxome
    $890
  • DNA in a shopping cart Complex Hereditary Spastic Paraplegia Panel
    Test Code
    Method
    Price
    2677
    Sequencing with CNV PGxome
    $1100
  • DNA in a shopping cart Distal Hereditary Motor Neuropathy Panel
    Test Code
    Method
    Price
    10353
    Sequencing with CNV PGxome
    $890
  • DNA in a shopping cart Hereditary Multiple Osteochondromas (HMO) Panel
    Test Code
    Method
    Price
    10085
    Sequencing with CNV PGxome
    $890
  • DNA in a shopping cart Hereditary Hearing Loss and Deafness Panel
    Test Code
    Method
    Price
    5063
    Sequencing with CNV PGxome
    $1290
  • DNA in a shopping cart Hereditary Sensory and Autonomic Neuropathy Panel
    Test Code
    Method
    Price
    10357
    Sequencing with CNV PGxome
    $960
  • DNA in a shopping cart Pure Hereditary Spastic Paraplegia Panel
    Test Code
    Method
    Price
    2679
    Sequencing with CNV PGxome
    $890
  • DNA in a shopping cart Hereditary Spastic Paraplegia Comprehensive Panel
    Test Code
    Method
    Price
    2673
    Sequencing with CNV PGxome
    $1310
  • DNA in a shopping cart Congenital Anomalies of the Gastrointestinal Tract Panel
    Test Code
    Method
    Price
    13377
    Sequencing with CNV PGxome
    $1350
Previous 1 ... 7 8 9 10 11 12 13 14 15 16 Next
  • GO BACK
    Test By Category
  • View All Tests
  • View All Panels
ORDER
Test Kits
Custom Panel CogSTART
Custom Panel

RESULTS KEY

  • Tests & Panels
  • Categories
  • Newsroom
  • Custom panels
  • Pages & Documents
  • Webinars

PreventionGenetics,
A wholly owned subsidiary of Exact Sciences Corp.

3800 S. Business Park Ave.
Marshfield, WI 54449
Contact Us

© 2023 PreventionGenetics. All rights reserved.

Quick links

Privacy Practices & Policies
Terms & Conditions
Contact Us
Careers
Sign Up For Newsletter

Follow us on

Also of Interest:
  • Genetic Tests by Category
  • PGxome ® - Whole Exome Sequencing
  • Genetic Tests by Disease
We use cookies and tracking to improve your browsing experience on our website, to analyze our website traffic, and to understand where our visitors are coming from. By browsing our website, you consent to this.