94417-3

LOINC 2.82

SLC6A4 gene 5-HTTLPR variant [Genotype] in Blood or Tissue by Molecular genetics method Nominal

SLC6A4 5-HTTLPR Geno Bld/T

Definition

  • A patient's genotype (e.g. S/S) for the 44-base pair promoter insertion/deletion polymorphism, 5-HTTLPR, in the SLC6A4 (solute carrier family 6 (neurotransmitter transporter), member 4) gene.

Component

  • SLC6A4 gene 5-HTTLPR variant

Specimen / system

  • Bld/Tiss

Class

  • MOLPATH.PHARMG

Property

  • Geno

Scale

  • Nom

Method

  • Molgen

Related names

  • 5HTT; 5-HTT; 5HTTLPR; 5-HTTLPR; 5-hydroxytryptamine transporter gene; Blood; Genetics; Heredity; Heritable; hSERT; HTT; Inherited; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.PHARMG; Nominal; OCD1; PCR; Point in time; Random; Serotonin transporter gene; SERT; SERT1; SLC6A4 5-HTTLPR; solute carrier family 6 (neurotransmitter transporter), member 4; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue

Index terms

  • 5-HTT
  • 5-HTTLPR
  • 5-hydroxytryptamine transporter gene
  • 5HTT
  • 5HTTLPR
  • Blood
  • Genetics
  • Heredity
  • Heritable
  • hSERT
  • HTT
  • Inherited
  • Molecular genetics
  • Molecular pathology
  • MOLPATH
  • MOLPATH.PHARMG
  • Nominal
  • OCD1
  • PCR
  • Point in time
  • Random
  • Serotonin transporter gene
  • SERT
  • SERT1
  • SLC6A4 5-HTTLPR
  • solute carrier family 6 (neurotransmitter transporter), member 4
  • Tissue
  • Tissue, unspecified
  • WB
  • Whole blood
  • Whole blood or Tissue