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LOINC 2.82

MCM6 gene c.-13910C>T and -13915T>G [Identifier] in Blood or Tissue by Molecular genetics method Nominal

MCM6 -13910C>T + -13915T>G Bld/T

Definition

  • Variants -13910C>T (rs4988235) and -13915T>G (rs41380347) located in intron 13 of the MCM6 gene are associated with hypolactasia, or lactose intolerance.

Component

  • MCM6 gene.c.-13910C>T & -13915T>G

Specimen / system

  • Bld/Tiss

Class

  • MOLPATH.MUT

Property

  • Prid

Scale

  • Nom

Method

  • Molgen

Related names

  • Blood; Genetics; Heredity; Heritable; Identity or presence; Inherited; Lactase; lactase persistence; lactase tolerance; MCG40308; MCM6 -13910C>T + -13915T>G; minichromosome maintenance complex component 6; Mis5; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Nominal; P105MCM; PCR; Point in time; Random; rs4988235; T prime; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue

Index terms

  • Blood
  • G
  • Genetics
  • Heredity
  • Heritable
  • Identity or presence
  • Inherited
  • Lactase
  • lactase persistence
  • lactase tolerance
  • MCG40308
  • MCM6 -13910C&gt
  • MCM6 gene.c.-13910C>T & -13915T>G
  • minichromosome maintenance complex component 6
  • Mis5
  • Molecular genetics
  • Molecular pathology
  • MOLPATH
  • MOLPATH.MUTATIONS
  • Nominal
  • P105MCM
  • PCR
  • Point in time
  • Random
  • rs4988235
  • T + -13915T&gt
  • T prime
  • Tissue
  • Tissue, unspecified
  • WB
  • Whole blood
  • Whole blood or Tissue