MTHFR C677T/A1298C Mutations Test

The MTHFR C677T/A1298C Mutations Test is a genetic test that helps determine if a person has mutations in the MTHFR gene. These mutations are associated with various health conditions, including cardiovascular disease, stroke, and neural tube defects in newborns.

At healthcare nt sickcare, we offer the MTHFR C677T/A1298C Mutations Test as part of our comprehensive range of genetic testing services. This test is useful in diagnosing and managing these health conditions.

During the test, a healthcare professional will draw a blood sample from the patient's arm or collect a saliva sample. The sample is then analysed in the lab to determine the presence of mutations in the MTHFR gene.

The MTHFR C677T/A1298C Mutations Test is a safe and non-invasive diagnostic test that can provide valuable information about a patient's genetic status. This test is recommended for individuals who have a family history of the above-mentioned health conditions or those who have experienced symptoms associated with these conditions.

At healthcare nt sickcare, we are committed to providing our patients with accurate and reliable genetic testing services in a comfortable and convenient environment. Our MTHFR C677T/A1298C Mutations Test is just one of the many tests we offer to help diagnose and manage genetic health conditions.