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: Galloway Mowat Syndrome (GAMOS) via the GON7������������������Gene

Search Results

  • DNA in a shopping cart Bernard-Soulier Syndrome via the GP9 Gene
    Test Code
    Method
    Price
    435
    Sanger Sequencing
    $370
    9227
    Sequencing with CNV PGxome
    $890
  • DNA in a shopping cart Aarskog-Scott Syndrome via the FGD1 Gene
    Test Code
    Method
    Price
    837
    Sanger Sequencing
    $940
    9887
    Sequencing with CNV PGxome
    $890
  • DNA in a shopping cart Beckwith-Wiedemann Syndrome via the CDKN1C Gene
    Test Code
    Method
    Price
    10005
    Sequencing with CNV PG-Select
    $640
  • DNA in a shopping cart Bohring-Opitz Syndrome via the ASXL1 Gene
    Test Code
    Method
    Price
    2298
    Sanger Sequencing
    $1280
    9827
    Sequencing with CNV PGxome
    $890
  • DNA in a shopping cart Brugada Syndrome 1 via the SCN5A Gene
    Test Code
    Method
    Price
    3113
    Sequencing with CNV PG-Select
    $640
  • DNA in a shopping cart Bamforth-Lazarus Syndrome via the FOXE1 Gene
    Test Code
    Method
    Price
    1582
    Sanger Sequencing
    $580
    8833
    Sequencing with CNV PGxome
    $890
  • DNA in a shopping cart Nijmegen Breakage Syndrome via the NBN Gene
    Test Code
    Method
    Price
    4837
    Sequencing with CNV PG-Select
    $540
  • DNA in a shopping cart Cohen Syndrome via the VPS13B (COH1) Gene
    Test Code
    Method
    Price
    15211
    Sequencing with CNV PG-Select
    $640
  • DNA in a shopping cart Congenital Myasthenic Syndrome via the CHRNE Gene
    Test Code
    Method
    Price
    6995
    Sequencing with CNV PG-Select
    $640
  • DNA in a shopping cart Congenital Myasthenic Syndrome via the MUSK Gene
    Test Code
    Method
    Price
    11477
    Sequencing with CNV PGxome
    $890
    406
    Sanger Sequencing
    $930
  • DNA in a shopping cart Congenital Nephrotic Syndrome via the NPHS1 Gene
    Test Code
    Method
    Price
    3097
    Sequencing with CNV PG-Select
    $640
  • DNA in a shopping cart Congenital Myasthenic Syndrome via the SYT2 Gene
    Test Code
    Method
    Price
    4419
    Sanger Sequencing
    $780
    8373
    Sequencing with CNV PGxome
    $890
  • DNA in a shopping cart Congenital Myasthenic Syndrome via the GFPT1 Gene
    Test Code
    Method
    Price
    4873
    Sequencing with CNV PG-Select
    $640
  • DNA in a shopping cart Congenital Myasthenic Syndrome via the COLQ Gene
    Test Code
    Method
    Price
    6997
    Sequencing with CNV PG-Select
    $640
  • DNA in a shopping cart Atrial Fibrillation Syndrome via the KCNA5 Gene
    Test Code
    Method
    Price
    2195
    Sanger Sequencing
    $250
    3967
    Sequencing with CNV PGxome
    $890
  • DNA in a shopping cart Atrial Fibrillation Syndrome via the NPPA Gene
    Test Code
    Method
    Price
    2201
    Sanger Sequencing
    $490
    3975
    Sequencing with CNV PGxome
    $890
  • DNA in a shopping cart Atrial Fibrillation Syndrome via the KCNE5 Gene
    Test Code
    Method
    Price
    11419
    Sequencing with CNV PGxome
    $890
    2920
    Sanger Sequencing
    $440
  • DNA in a shopping cart Atrial Fibrillation Syndrome via the MYL4 Gene
    Test Code
    Method
    Price
    5117
    Sanger Sequencing
    $710
    8463
    Sequencing with CNV PGxome
    $890
  • DNA in a shopping cart Ataxia Telangiectasia Syndrome via the ATM Gene
    Test Code
    Method
    Price
    3049
    Sequencing with CNV PG-Select
    $540
  • DNA in a shopping cart Pulmonary Fibrosis Syndrome via the SFTPA2 Gene
    Test Code
    Method
    Price
    2307
    Sanger Sequencing
    $690
Previous 1 ... 9 10 11 12 13 14 15 16 17 18 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.