Search Tests - PreventionGenetics

Menu

Menu
  • Testing

      Test Menu

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

      Test Information

      • Test Methods
      • Variant Interpretation
      • Family Testing
      • Re-analysis Policy
      • Extract and Hold
  • Sponsored Testing

      Partner Programs

      • Collaboration
      • Sponsored Testing
      • Clinical Trials and Research Studies
  • Billing

      Billing Information

      • Billing Policy
      • In-network Health Plans
      • Utilization Management
      • FAQs
      • Forms
  • 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
  • About Us

      PreventionGenetics

      • About PreventionGenetics
      • Genetics Experts
      • Quality & Value
      • Publications
      • Licenses and Certificates
      • Webinars
      • 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
      • PGmax
      • Custom Panels
      • Tests by Category
      • How To Order
      • Targeted Variants
      • Prenatal
      • All Tests
      • Tests by Disease

      Test Information

      • Test Methods
      • Variant Interpretation
      • Family Testing
      • Re-analysis Policy
      • Extract and Hold
  • |
  • Sponsored Testing

      Partner Programs

      • Collaboration
      • Sponsored Testing
      • Clinical Trials and Research Studies
  • |
  • Billing

      Billing Information

      • Billing Policy
      • In-network Health Plans
      • Utilization Management
      • FAQs
      • Forms
  • |
  • 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
  • |
  • About Us

      PreventionGenetics

      • About PreventionGenetics
      • Genetics Experts
      • Quality & Value
      • Publications
      • Licenses and Certificates
      • Webinars
      • 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: Autosomal Dominant DOPA-Responsive Dystonia via the GCH1 Gene

Search Results

  • DNA in a shopping cart Dystonia Panel
    Test Code
    Method
    Price
    3017
    Sequencing with CNV PGxome
    $990
  • DNA in a shopping cart Hyperphenylalaninemia Panel
    Test Code
    Method
    Price
    3403
    Sequencing with CNV PGxome
    $990
  • DNA in a shopping cart Parkinson Disease Panel
    Test Code
    Method
    Price
    10337
    Sequencing with CNV PGxome
    $990
  • DNA in a shopping cart Parkinson Disease and Parkinsonism Panel
    Test Code
    Method
    Price
    10623
    Sequencing with CNV PGxome
    $990
  • DNA in a shopping cart Complex Hereditary Spastic Paraplegia Panel
    Test Code
    Method
    Price
    2677
    Sequencing with CNV PGxome
    $990
  • DNA in a shopping cart Hereditary Spastic Paraplegia Comprehensive Panel
    Test Code
    Method
    Price
    2673
    Sequencing with CNV PGxome
    $1290
  • DNA in a shopping cart Sepiapterin Reductase (SR) Deficiency via the SPR Gene
    Test Code
    Method
    Price
    1871
    Sanger Sequencing
    $540
    9043
    Sequencing with CNV PGxome
    $990
  • DNA in a shopping cart Infantile Parkinsonism-Dystonia Panel
    Test Code
    Method
    Price
    12609
    Sequencing with CNV PGxome
    $990
  • DNA in a shopping cart Thiamine Responsive Megaloblastic Anemia via the SLC19A2 Gene
    Test Code
    Method
    Price
    2034
    Sanger Sequencing
    $650
    9997
    Sequencing with CNV PGxome
    $990
  • DNA in a shopping cart Dystonia via the GNAL Gene
    Test Code
    Method
    Price
    5415
    Sequencing with CNV PGxome
    $990
  • DNA in a shopping cart Dystonia via the THAP1 Gene
    Test Code
    Method
    Price
    5417
    Sequencing with CNV PGxome
    $990
    2740
    Sanger Sequencing
    $580
  • DNA in a shopping cart Dystonia via the ANO3 Gene
    Test Code
    Method
    Price
    5293
    Sequencing with CNV PGxome
    $990
  • DNA in a shopping cart Autosomal Dominant Retinitis Pigmentosa via the SNRNP200 Gene
    Test Code
    Method
    Price
    4927
    Sequencing with CNV PGxome
    $990
  • DNA in a shopping cart Autosomal Dominant Retinitis Pigmentosa via the PRPF6 Gene
    Test Code
    Method
    Price
    4915
    Sequencing with CNV PGxome
    $990
  • DNA in a shopping cart Autosomal Dominant Congenital Cataracts via the MIP Gene
    Test Code
    Method
    Price
    2927
    Sanger Sequencing
    $580
    3929
    Sequencing with CNV PGxome
    $990
  • DNA in a shopping cart SYNJ1-Related Disorders via the SYNJ1 Gene
    Test Code
    Method
    Price
    13021
    Sequencing with CNV PGxome
    $990
  • DNA in a shopping cart PGmaxTM - Comprehensive Movement Disorders Panel
    Test Code
    Method
    Price
    16004
    Sequencing with CNV PGxome
    $1790
  • DNA in a shopping cart Deafness, Autosomal Dominant 44 (DFNA44) via the CCDC50 Gene
    Test Code
    Method
    Price
    11151
    Sequencing with CNV PGxome
    $990
    2242
    Sanger Sequencing
    $970
  • DNA in a shopping cart Deafness, Autosomal Dominant 2A (DFNA2A) via the KCNQ4 Gene
    Test Code
    Method
    Price
    11423
    Sequencing with CNV PGxome
    $990
  • DNA in a shopping cart Centronuclear Myopathy-3, Autosomal Dominant via the MYF6 Gene
    Test Code
    Method
    Price
    924
    Sanger Sequencing
    $540
    8955
    Sequencing with CNV PGxome
    $990
1 2 3 4 5 6 7 8 9 10 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

© 2025 PreventionGenetics. All rights reserved.

Quick links

Privacy Practices & Policies
HIPAA Compliance
Do Not Sell
Contact Us
Careers
Get on Our Mailing List

Follow us on