Genomic Unity® Lynch Syndrome Analysis

Genomic Unity® Lynch Syndrome Analysis is an effective test for Lynch Syndrome, also known as hereditary non-polyposis colorectal cancer (HNPCC), an inherited cancer syndrome that is associated with genetic predisposition to different types of cancer.

Order this test when the patient presents with symptoms of Lynch Syndrome, and you'd like the option to reflex up to Genomic Unity® Whole Genome Analysis.

  • Sequencing analysis of Lynch Syndrome associated genes
  • Del/dup analysis of Lynch Syndrome associated genes

Optionally includes:

  • Reflex to Genomic Unity® Whole Genome Analysis or Genomic Unity® Exome Analysis

EPCAM, MLH1, MSH2, MSH6, PMS2

SNVs and Indels up to 50bp
99.7% sensitivity
99.6% positive predictive value

Structural variants:
96% clinical sensitivity

81292, 81294, 81295, 81297, 81298, 81300, 81317, 81319, 81479

The CPT codes provided are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payer being billed.

Blood - 5ml
Saliva - contact us for a kit
gDNA - 5μg

Turn around time is 6-8 weeks from sample receipt.