ARUP's Laboratory Test Directory

0051648: HNPCC/Lynch Syndrome, Family Specific Mutation

[ image for: Patient History for HNPCC/Lynch Syndrome Testing]
Patient History for HNPCC/Lynch Syndrome Testing
  

Test Mnemonic: HNPCC FSM
Methodology: Polymerase Chain Reaction/Sequencing or Multiplex Ligation Probe Amplification

Performed: Varies

Reported: Within 28 days

Specimen Required:  
Collect: Please contact ARUP's genetic counselor at (800) 242-2787 extension 3949 prior to test submission. HNPCC/Lynch Syndrome FSM specific forms are available upon request.

Interpretive Data:
Refer to report.

This test is performed pursuant to an agreement with Roche Molecular Systems, Inc.



Counseling and informed consent are recommended for genetic testing. Consent forms are available online at www.aruplab.com.

Please refer to Statement C in the Compliance Statements section in the front of the Laboratory Test Directory.



Note:
Available for MLH1, MSH2, and MSH6 genes.

CPT Code(s):
Sequencing: 83891 Isolation; 83898 Amplification; 83904 Sequencing; 83909 Capillary electrophoresis; 83912 Interpretation and report or MLPA: 83891 Isolation; 83896 Nucleic Acid Probes; 83898 Amplification; 83914 Extension; 83909 Capillary Electrophoresis; 83912 Interpretation and report