Yerevan
EN
Lab tests
18-008

Methylenetetrahydrofolate reductase (MTHFR). Detection of mutation A1298C (Glu429Ala)

Description

The marker is associated with changes in methionine metabolism. It is investigated to identify genetic predisposition to hyperhomocysteinemia, vascular diseases, anemia, ischemic heart disease, ischemic stroke, hypertension, thrombosis, retinal artery occlusion, preeclampsia, various forms of cancer, primary glaucoma, migraines, depression, schizophrenia, and in the fetus: neural tube defects, Down syndrome, and cleft lip. It is informative for prescribing folic acid and for dietary recommendations (vitamin K). OMIM: 607093.

Period of execution

Within 6 days. The specified time does not include the day of biomaterial collection

Biomaterial type

  • Buccal (cheek) epithelium
  • Venous blood
Total price
5495 ֏
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