Keyword Analysis & Research: mthfr labcorp


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mthfr labcorp0.370.6522510013
mthfr1.850.71526105
labcorp1.110.68031407

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mthfr labcorp0.961398596

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  • 511238: Methylenetetrahydrofolate Reductase (MTHFR ... - Labcorp

    labcorp.com

    https://www.labcorp.com/tests/511238/methylenetetrahydrofolate-reductase-mthfr-thermolabile-variant-dna-analysis

    WEBReduced enzyme activity of methylenetetrahydrofolate reductase (MTHFR) is a genetic risk factor for hyperhomocysteinemia, particularly when serum folate levels are low. There are two common variants in the MTHFR gene that can decrease enzyme activity: c.665C>T (p. Ala222Val), legacy name C677T, and c.1286A>C (p. Glu429Ala), legacy name A1298C.

    DA: 29 PA: 56 MOZ Rank: 90

  • Methylenetetrahydrofolate Reductase (MTHFR) C677T and A1298C - Labcorp

    labcorp.com

    https://specialtytesting.labcorp.com/tests/511238/methylenetetrahydrofolate-reductase-mthfr-c677t-and-a1298c

    WEBLabCorp test details for Methylenetetrahydrofolate Reductase (MTHFR) C677T and A1298C 511238 Methylenetetrahydrofolate Reductase (MTHFR) C677T and A1298C | Specialty Testing | Laboratory Corporation of America

    DA: 30 PA: 97 MOZ Rank: 31

  • Genetic Thrombophilia | Labcorp

    labcorp.com

    https://www.labcorp.com/resource/genetic-thrombophilia

    WEBGenetic testing is useful for the diagnosis or confirmation of MTHFR, factor V Leiden, and the prothrombin 20210 mutations. Regardless of clinical status, genetic testing can be definitive because the patient's DNA remains constant. Antigen and activity levels must be measured to diagnose the other congenital thrombotic conditions.

    DA: 6 PA: 71 MOZ Rank: 90

  • MTHFR Gene May Be Causing Your Fatigue, Headaches, Depression, and More

    universityhealthnews.com

    https://universityhealthnews.com/daily/energy-fatigue/the-mthfr-test-detects-a-genetic-defect-that-may-be-causing-your-fatigue-headaches-depression-and-more/

    WEBApr 14, 2020 · The test is commonly available through conventional laboratories such as LabCorp, as well as through popular functional laboratories such as Spectracell and Doctor’s Data. The easiest and least expensive option, however, may be to go through a company that offers complete genetic profiles, such as 23andMe.

    DA: 21 PA: 98 MOZ Rank: 43

  • MTHFR Mutation Test: MedlinePlus Medical Test

    medlineplus.gov

    https://medlineplus.gov/lab-tests/mthfr-mutation-test/

    WEBAn MTHFR gene test is used to look for the two most common MTHFR changes called C677T and A1298C. It's possible to have one or both of these gene changes without having any health problems. An MTHFR gene test may be done alone or as part of a group of genetic tests. The test may be used to:

    DA: 51 PA: 42 MOZ Rank: 78

  • MTHFR mutation: Symptoms, testing, and treatment - Medical News Today

    medicalnewstoday.com

    https://www.medicalnewstoday.com/articles/326181

    WEBNov 24, 2023 · Contacting a doctor. Summary. Methylenetetrahydrofolate reductase (MTHFR) is an enzyme that breaks down the amino acid homocysteine. If the MTHFR gene that codes for this enzyme mutates,...

    DA: 72 PA: 2 MOZ Rank: 94

  • Methylenetetrahydrofolate Reductase (MTHFR), DNA Mutation …

    clevelandheartlab.com

    https://www.clevelandheartlab.com/tests/mthfr/

    WEBAug 22, 2013 · Clinical Significance: The Methylenetetrahydrofolate Reductase (MTHFR) enzyme plays a major role in homocysteine metabolism and contains several known polymorphisms, of which the most common is C677T. This mutation is reported to reduce MTHFR activity, resulting in hyperhomocysteinemia.

    DA: 10 PA: 34 MOZ Rank: 72

  • Methylenetetrahydrofolate Reductase ( MTHFR ) 2 Variants

    aruplab.com

    https://ltd.aruplab.com/Tests/Pub/0055655

    WEBAug 15, 2022 · MTHFR variants are only one contributing factor. Methodology: Polymerase chain reaction (PCR) and fluorescence monitoring. Analytical Sensitivity & Specificity: 99 percent. Limitations: Only two MTHFR gene variants (c.665C>T and c.1286A>C) are tested. Diagnostic errors can occur due to rare sequence variations.

    DA: 89 PA: 96 MOZ Rank: 95

  • Methylenetetrahydrofolate Reductase Deficiency - Medical …

    nih.gov

    https://www.ncbi.nlm.nih.gov/books/NBK66131/

    WEBMar 8, 2012 · Methylenetetrahydrofolate Reductase (MTHFR) Deficiency is the most common genetic cause of elevated levels of homocysteine in the plasma (hyperhomocysteinemia). The MTHFR enzyme plays an important role in processing amino acids, specifically, the conversion of homocysteine to methionine.

    DA: 95 PA: 93 MOZ Rank: 4

  • Methylenetetrahydrofolate Reductase (MTHFR), DNA Analysis

    questdiagnostics.com

    https://www.questdiagnostics.com/healthcare-professionals/clinical-education-center/faq/faq66

    WEBWhat is methylenetetrahydrofolate reductase (MTHFR) DNA analysis, and what conditions are associated with the variants tested? MTHFR DNA analysis tests for the presence or absence of two variants in the MTHFR gene: C677T and A1298C.

    DA: 15 PA: 87 MOZ Rank: 80