MTHFR Gene Mutation, C677T & A1298C SNPs, blood spot (code 5018)
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MTHFR Genetic Mutation-Blood spot test identifies a unique gene variation which may severely impact how well the body metabolises folate and folic acid, b vitamins which may lead to reduced ability to break down homocysteine in which may lead to increased risk for heart related health concerns.
Interested to learn more about other nutrition-related genetic mutations? You may be interested in the more comprehensive Fitgenes Health & Wellbeing Profile offered by Dr Kathleen- which includes the MTHFR along with analysis of 57 other genetic mutations.
Test booking required
NZD166.40
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MTHFR Gene Mutation, C677T & A1298C SNPs, blood spot (code 5018)
