MTHFR C677T & A1298C Mutations Test
MTHFR C677T & A1298C Mutations Test
Direct answer: This genetic test detects common MTHFR gene mutations linked to folate metabolism and elevated homocysteine risk.
The MTHFR C677T & A1298C Mutations Test is a molecular genetics test that identifies variations in the Methylenetetrahydrofolate Reductase (MTHFR) gene. The MTHFR enzyme plays a key role in processing folate (vitamin B9) and regulating homocysteine levels in the blood. Detecting C677T and A1298C mutations helps assess inherited risk for impaired folate metabolism, cardiovascular concerns, pregnancy complications, and certain neurological conditions.
This test is available at healthcare nt sickcare with home collection facility in Pune and direct walk-in sample submission at our Aundh centre. Samples are processed through NABL-accredited partner laboratories with secure digital reporting for patients across Pune, Maharashtra.
Who Should Consider This Test?
Direct answer: Individuals with high homocysteine levels, recurrent pregnancy loss, or family history of clotting disorders.
This test is commonly advised for unexplained blood clotting, repeated miscarriages, infertility evaluation, cardiovascular risk assessment, or when homocysteine levels are persistently elevated. Genetic insight supports personalised nutritional and clinical guidance.
Patient Resources
Frequently Asked Questions
When should I do the MTHFR mutations test?
Why is this test advised?
Is fasting required before this test?
What symptoms may prompt this test?
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Original: $6,999.00
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Description
MTHFR C677T & A1298C Mutations Test
Direct answer: This genetic test detects common MTHFR gene mutations linked to folate metabolism and elevated homocysteine risk.
The MTHFR C677T & A1298C Mutations Test is a molecular genetics test that identifies variations in the Methylenetetrahydrofolate Reductase (MTHFR) gene. The MTHFR enzyme plays a key role in processing folate (vitamin B9) and regulating homocysteine levels in the blood. Detecting C677T and A1298C mutations helps assess inherited risk for impaired folate metabolism, cardiovascular concerns, pregnancy complications, and certain neurological conditions.
This test is available at healthcare nt sickcare with home collection facility in Pune and direct walk-in sample submission at our Aundh centre. Samples are processed through NABL-accredited partner laboratories with secure digital reporting for patients across Pune, Maharashtra.
Who Should Consider This Test?
Direct answer: Individuals with high homocysteine levels, recurrent pregnancy loss, or family history of clotting disorders.
This test is commonly advised for unexplained blood clotting, repeated miscarriages, infertility evaluation, cardiovascular risk assessment, or when homocysteine levels are persistently elevated. Genetic insight supports personalised nutritional and clinical guidance.
Patient Resources
Frequently Asked Questions
When should I do the MTHFR mutations test?
Why is this test advised?
Is fasting required before this test?
What symptoms may prompt this test?
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