MTHFR (Methylenetetrahydrofolate Reductase) is a vital gene that provides the instructions for making an enzyme your body needs to process Folate (Vitamin B9) and Folic acid to their active state called 5-Methyltetrahydrofolate (5-MTHF).
Methyltetrahydrofolate is essential for red blood cell formation, DNA synthesis and repair, and the efficient utilization of other nutrients, such as Vitamin B12.
It is also important in converting homocysteine into methionine. Methionine is a fundamental building block for proteins and is essential for maintaining a healthy, low-inflammation environment in the body. Failure to convert homocysteine may result in adverse health conditions
Our MTHFR genetic test is a valuable tool for individuals seeking to understand how specific gene variants may impact the conversion of folate and folic acid into their biologically active form. We test two common alleles in the MTHFR gene, known as C677T and A1298C. Certain variants of these alleles result in your MTHFR enzyme becomes less active.
While identifying your MTHFR status can inform personalized supplementation, it is important to note that clinical evidence linking these variants to specific health outcomes is still emerging. Consequently, test results should be interpreted alongside professional medical advice and a comprehensive lifestyle assessment.
