Identifies mutations in the MTHFR gene, which influence homocysteine regulation and the metabolism of folate (vitamin B9) and other B vitamins. These nutrients are essential for metabolic and cellular functions. MTHFR mutations are associated with increased risk of heart disease, mental health issues, dementia, immune dysfunction, certain cancers, miscarriage, preeclampsia, and certain congenital disabilities. Ideal for: Family history of MTHFR mutations, elevated homocysteine, cardiovascular concerns, or those planning for pregnancy May help explain: Fatigue, depression, cognitive changes, or recurrent miscarriages Next steps after results: Targeted nutrition and supplementation to support folate and B-vitamin pathways, and improving gut health with probiotics, prebiotics, and fiber Suggested frequency: One-time genetic test Biomarker (1): MTHFR gene (methylenetetrahydrofolate reductase)
