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MTHFR (C677T) Mutation Analysis

The MTHFR mutation is one of the genetic risk factors for thrombosis. Indications for MTHFR testing as part of the screening for thrombophilia include: venous thromboembolism (especially if in an unusual site), deep vein thrombosis during pregnancy, venous thromboembolism while on oral contraceptive, fetal death after 10 weeks gestation, fetal growth restriction and/or preclampsia, and/or family history of stroke, pulmonary embolus, deep vein thrombosis in first degree relatives under age 50.

CPT Codes:

83893(1), 83894(1), 83896(2), 83898(2), 83912(1)


Specimen Requirements:

Blood:

Adult: 10 ml whole blood in ACD-A (yellow-top) or EDTA (lavender-top) tube.

Turnaround Time:

7-10 days


Client Services: Reproductive/Genetics   800-848-4436

Specimen Services/Pickup:  877-246-1226

Reproductive/Genetics Client Services

Tel: 800-848-4436