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Polyposis Sequencing Panel

Genesys Diagnostics
SKU: GDI08

$3,200.00 per test

Helps individuals who want to determine their risk of Lynch Syndrome by using the latest next generation sequencing because unlike any other Clinical Diagnostics marketplace Meenta offers unfettered access to validated tests.

 

 

 

 

 

Available on backorder

Helps individuals who want to determine their risk of Lynch Syndrome by using the latest next generation sequencing because unlike any other Clinical Diagnostics marketplace Meenta offers unfettered access to validated tests.

 

 

 

 

 

The Fine Print

Purpose: Detect risk of Polysosis disease

Benefits:

  • Analyzes genes involved in Hereditary Polyposis Syndrome
  • Helps inform helpful healthcare and lifestyle changes
  • Reveals genetic risk in yourself and close relatives
  • Comprehensive genetic test
  • Outlines hereditary mutations that can reveal increased risk to future generations

Sample type: Cheek swab

Technology: Next Generation Sequencing

Turnaround time: 3-4 weeks from receipt in lab

A polyp is a growth that protrudes from a mucous membrane.  If someone has a hereditary condition that causes an increased risk of polyps in the digestive tract, usually in the colon and/or rectum, it is called Polyposis.  There are various shapes of polyps that may occur. The thought is that polyps in the tract should be removed surgically to prevent a polyp to progressing to cancer.  Currently, there are two methods to determine polyposis: endoscopy or genetic testing.

The same types of polyps that develop in hereditary polyposis syndrome can also develop in individuals without it. Compared to the general population, people with this syndrome typically have higher numbers of polyps, develop them at younger ages, and often develop them more quickly.

 
This test includes:  APC, MUTYH

How do I interpret the results?

Genetic counseling is generally recommended for any individual taking this test and their family. A medical provider can request reanalysis of the variants, and this is recommended on an annual basis. Data from this next-generation sequencing analysis can be reassessed for the presence of any new variants that may be newly linked to established genes or to newly characterized genes and/or disorders identified since the data used in this report was generated. A charge may be applied for reanalysis. Please contact support@meenta.io for more information at the time reanalysis is requested.
Cheek swab in viral transport media shipped at room temperature

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