MTHFR Mutations C677T / A1298C is a genetic test used to identify two common variations in the MTHFR gene: C677T and A1298C. The MTHFR gene plays an important role in processing folate and regulating homocysteine levels in the body. These genetic variations may affect the efficiency of folate metabolism and, in some individuals, may be associated with altered homocysteine levels. The test is performed using a blood sample and usually does not require fasting. It may be advised in specific clinical situations based on medical history, laboratory findings, or family history. Results should be interpreted by a qualified healthcare professional along with other clinical information.
Clinical purpose and recommended diagnostic indicators
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Fasting is not mandatory
Water intake is completely permitted unless specified otherwise
Popular health packages and diagnostic profiles
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