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