94414-0

LOINC 2.82

MTHFR gene c.677C>T and c.1298A>C [Genotype] in Blood or Tissue by Molecular genetics method Nominal

MTHFR c.677C>T + 1298A>C Geno Bld/T

Definition

  • The patient's genotype for c.665C>T (rs1801133) and c.1298A>C (rs1801131) variants in the MTHFR gene.

Component

  • MTHFR gene.c.677C>T & c.1298A>C

Specimen / system

  • Bld/Tiss

Class

  • MOLPATH.PHARMG

Property

  • Geno

Scale

  • Nom

Method

  • Molgen

Related names

  • 5,10-methylenetetrahydrofolate reductase gene; Blood; c.665C>T; C665T; C677T; Genetics; Heredity; Heritable; Inherited; methylenetetrahydrofolate reductase (NAD(P)H); Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.PHARMG; MTHFR c.677C>T; MTHFR c.677C>T + 1298A>C; NADPH; Nominal; p.A222V; p.Ala222Val; PCR; Point in time; Random; T prime; Tissue; Tissue, unspecified; Vascular risk; WB; Whole blood; Whole blood or Tissue

Index terms

  • 5,10-methylenetetrahydrofolate reductase gene
  • Blood
  • C
  • c.665C&gt
  • C665T
  • C677T
  • Genetics
  • Heredity
  • Heritable
  • Inherited
  • methylenetetrahydrofolate reductase (NAD(P)H)
  • Molecular genetics
  • Molecular pathology
  • MOLPATH
  • MOLPATH.PHARMG
  • MTHFR c.677C&gt
  • MTHFR gene.c.677C>T & c.1298A>C
  • NADPH
  • Nominal
  • p.A222V
  • p.Ala222Val
  • PCR
  • Point in time
  • Random
  • T
  • T + 1298A&gt
  • T prime
  • Tissue
  • Tissue, unspecified
  • Vascular risk
  • WB
  • Whole blood
  • Whole blood or Tissue