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Test Code Billings Clinic:8218 ARUP:0055655 Methylenetetrahydrofolate Reductase (MTHFR) 2 Variants

Performing Laboratory

ARUP Laboratories

Useful For

Background Information for Methylenetetrahydrofolate Reductase (MTHFR), 2 Variants:
Characteristics: 
Variants in the MTHFR gene may reduce enzyme activity contributing to hyperhomocysteinemia. Although hyperhomocysteinemia was previously reported to be a risk factor for many conditions, especially venous thrombosis and cardiovascular disease, recent meta-analysis casts doubt on whether lifelong moderate homocysteine elevation has an effect on cardiovascular disease. The American College of Medical Genetics Practice Guidelines indicate that individuals with elevated homocysteine and two copies of the c.665C>T variant have an odds ratio of 1.27 for venous thromboembolism. Thus, they recommend MTHFR genotyping not be ordered as part of a routine evaluation for recurrent pregnancy loss or thrombophilia due to questionable clinical significance.

Methodology

Polymerase Chain Reaction (PCR)/Fluorescence Monitoring

Specimen Requirements

Lavender (EDTA), pink (K2EDTA), or yellow (ACD Solution A or B).

Transport 3 mL whole blood. (Min: 1 mL)

Refrigerated.

Storage/Stability

Ambient: 72 hours; Refrigerated: 1 week; Frozen: 1 month

 

LOINC Code

Component Test Code* Component Chart Name LOINC
0055657 MTHFR Variant: c.665C>T 28005-7
0055658 MTHFR Variant: c.1286A>C 28060-2
0055660 MTHFR Interpretation 21709-1
2001331 MTHFR PCR Specimen 31208-2

Reject Due To

Plasma or serum. Heparinized specimens. Frozen specimens in glass collection tubes.

Day(s) Test Set Up

Sun-Sat

CPT Code

81291