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