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HNPCC (MLH1 & MSH2) Mutation
SKU: MD-NLB047 Categories: , , , , , , , , , , Tags: , , , , , ,

In Stock

HNPCC (MLH1 & MSH2) Mutation

฿40,000.00

Additional information

Also Known As

Lynch Syndrome Genetic Test, HNPCC Testing
Specimen

EDTA whole blood 10 – 15 ml.
Turnaround Time

3 month
Test Code

MD-NLB047
Test Type

Special
Related Tests

MSI Testing, Tumor Marker Panel

A genetic test that detects mutations in the MLH1 and MSH2 genes associated with Lynch syndrome (hereditary nonpolyposis colorectal cancer). It helps in assessing cancer risk, especially for colorectal and endometrial cancer.

Product tags: Cancer, Fatigue, Genetic Disorders, HNPCC Testing, Lynch Syndrome Genetic Test, None, Unexplained Weight Loss
Diseases: Cancer, Genetic Disorders
Symptoms: Fatigue, Unexplained Weight Loss
Habits: None
Age Groups: Adults
Specimens: EDTA Whole Blood
Diagnostic Methods: DHPLC, DNA Sequencing, PCR
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Description

A genetic test that detects mutations in the MLH1 and MSH2 genes associated with Lynch syndrome (hereditary nonpolyposis colorectal cancer). It helps in assessing cancer risk, especially for colorectal and endometrial cancer.

This lab test includes home sample collection via a provided kit or by a clinician, and you’ll receive a comprehensive physical health report with your results.

Additional information

Also Known As

Specimen

Turnaround Time

Test Code

Test Type

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