ARUP's Laboratory Test Directory

HNPCC/Lynch Syndrome, Family Specific Mutation : 0051648
[ image for: Patient History for HNPCC/Lynch Syndrome Testing]
Patient History for HNPCC/Lynch Syndrome Testing
  


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 3439 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.





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
 
 

 

 

 
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