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The MTHFR C677T & A1298C Detection Lab Test is a genetic screening tool that identifies mutations in the MTHFR gene, which can impact folate metabolism, homocysteine levels, and overall health. Key features include accurate detection of both common MTHFR variants (C677T and A1298C) through a simple saliva or blood sample.
The MTHFR Mutation (C677T) Analysis is a genetic test that identifies the presence of the C677T variant in the MTHFR gene, which can impact folate metabolism and homocysteine levels. Key features include accurate DNA analysis using a simple saliva or cheek swab sample, fast turnaround time, and clear, actionable results. Benefits include personalized insights into potential health risks such as cardiovascular issues, fertility challenges, and neurological conditions, enabling targeted lifestyle and nutritional interventions. Its unique selling point lies in empowering individuals with genetic knowledge to make informed health decisions and optimize wellness through precision nutrition.