M0146
MTHFR Mutation Detection
Test Details: This test is used to determine genetic contribution to hyperhomocysteinemia for individuals with elevated plasma homocysteine. The common MTHFR gene variant c.677C>T may reduce MTHFR enzyme activity and contribute to a mild to moderate increase in plasma homocysteine concentrations.
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Category
Molecular Genetics
Pre-test Information
Clinical history is mandatory.
Report Delivery
4 working days
Gender
All
Organ
Blood
MTHFR Mutation Detection
4400
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