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 Peutz-Jeghers Syndrome via the STK11 Gene
    Test Code
    Method
    Price
    7525
    Sequencing with CNV PG-Select
    $540
  • DNA in a shopping cart Peeling Skin Syndrome via the TGM5 Gene
    Test Code
    Method
    Price
    2096
    Sanger Sequencing
    $870
    8253
    Sequencing with CNV PGxome
    $890
  • DNA in a shopping cart Dubin-Johnson Syndrome via the ABCC2 Gene
    Test Code
    Method
    Price
    15217
    Sequencing with CNV PG-Select
    $640
  • DNA in a shopping cart Creatine Deficiency Syndrome via the SLC6A8 Gene
    Test Code
    Method
    Price
    7831
    Sequencing with CNV PG-Select
    $640
  • DNA in a shopping cart Bardet-Biedl Syndrome via the BBS12 Gene
    Test Code
    Method
    Price
    7589
    Sequencing with CNV PG-Select
    $640
  • DNA in a shopping cart Dias-Logan Syndrome via the BCL11A Gene
    Test Code
    Method
    Price
    15233
    Sequencing with CNV PG-Select
    $640
  • DNA in a shopping cart Bardet-Biedl Syndrome via the BBS5 Gene
    Test Code
    Method
    Price
    15147
    Sequencing with CNV PG-Select
    $640
  • DNA in a shopping cart Bardet-Biedl Syndrome via the BBS2 Gene
    Test Code
    Method
    Price
    6955
    Sequencing with CNV PG-Select
    $640
  • DNA in a shopping cart Conradi-Hunermann syndrome via the EBP Gene
    Test Code
    Method
    Price
    8935
    Sequencing with CNV PGxome
    $890
    781
    Sanger Sequencing
    $560
  • DNA in a shopping cart 3-M Syndrome via the CCDC8 Gene
    Test Code
    Method
    Price
    2882
    Sanger Sequencing
    $580
    8823
    Sequencing with CNV PGxome
    $890
  • DNA in a shopping cart Bardet-Biedl Syndrome via the BBS4 Gene
    Test Code
    Method
    Price
    6957
    Sequencing with CNV PG-Select
    $640
  • DNA in a shopping cart Creatine Deficiency Syndrome via the GAMT Gene
    Test Code
    Method
    Price
    242
    Sanger Sequencing
    $610
    9615
    Sequencing with CNV PGxome
    $890
  • DNA in a shopping cart Creatine Deficiency Syndrome via the GATM Gene
    Test Code
    Method
    Price
    241
    Sanger Sequencing
    $690
    11881
    Sequencing with CNV PGxome
    $890
  • DNA in a shopping cart Autoimmune Lymphoproliferative Syndrome via the FAS Gene
    Test Code
    Method
    Price
    1648
    Sanger Sequencing
    $810
    8323
    Sequencing with CNV PGxome
    $890
  • DNA in a shopping cart Bardet-Biedl Syndrome via the BBS7 Gene
    Test Code
    Method
    Price
    7591
    Sequencing with CNV PG-Select
    $640
  • DNA in a shopping cart Barth Syndrome via the TAFAZZIN/TAZ Gene
    Test Code
    Method
    Price
    149
    Sanger Sequencing
    $680
    8525
    Sequencing with CNV PGxome
    $890
  • DNA in a shopping cart 3-M Syndrome via the CUL7 Gene
    Test Code
    Method
    Price
    11221
    Sequencing with CNV PGxome
    $890
    624
    Sanger Sequencing
    $1320
  • DNA in a shopping cart Adams-Oliver Syndrome via the DOCK6 Gene
    Test Code
    Method
    Price
    11255
    Sequencing with CNV PGxome
    $890
    2292
    Sanger Sequencing
    $2110
  • DNA in a shopping cart Alagille Syndrome-1 via the JAG1 Gene
    Test Code
    Method
    Price
    15253
    Sequencing with CNV PG-Select
    $640
  • DNA in a shopping cart Bardet-Biedl Syndrome via the BBS10 Gene
    Test Code
    Method
    Price
    7587
    Sequencing with CNV PG-Select
    $640
Previous 1 ... 10 11 12 13 14 15 16 17 18 19 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.