GTR Home > Tests > KRAS-Related Noonan Syndrome

Overview

Test order codeHelp: 2340

Test name

Help

KRAS-Related Noonan Syndrome

Purpose of the test

Help

This is a clinical test intended for Help: Diagnosis, Mutation Confirmation

Condition

Help

1 condition tested. Click Indication tab for more information.

Methodology

Help
Molecular Genetics
CSequence analysis of the entire coding region
Bi-directional Sanger Sequence Analysis

Summary of what is tested

1 genes and variants. Click Methodology tab for more information.

Genes

Clinical validity

Help

Mutations in KRAS account for approximately 2-5% of Noonan syndrome cases.

Citations

Not provided

Clinical utility

Help

Not provided

Testing strategy

Help

Test can be run as individual gene sequence analysis, as part of a panel, or specific site analysis.

How to order

Help

Order URL Help: http://ambrygen.com/forms

Test services

Help
  • Clinical Testing/Confirmation of Mutations Identified Previously, Order code: 2340
  • Custom Prenatal Testing
  • Custom mutation-specific/Carrier testing

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.

Support Center