47997-2

LOINC 2.82

Genetic variant clinical significance [Interpretation] in Blood or Tissue by Molecular genetics method

Genetic variant clin sig Bld/T-Imp

Component

  • Genetic variant clinical significance

Specimen / system

  • Bld/Tiss

Class

  • MOLPATH.MISC

Property

  • Imp

Scale

  • Nom

Method

  • Molgen

Related names

  • Blood; Genetic variant clin sig; Genetics; Genomic; Impression; Impression/interpretation of study; Impressions; Interp; Interpretation; MISC; Miscellaneous molecular pathology; Molecular genetics; Molecular pathology; MOLPATH; Nominal; PCR; Point in time; Random; Tissue; Tissue, unspecified; Variant Interpretation; WB; Whole blood; Whole blood or Tissue

Index terms

  • Blood
  • Genetic variant clin sig
  • Genetics
  • Genomic
  • Impression
  • Impression/interpretation of study
  • Impressions
  • Interp
  • Interpretation
  • MISC
  • Miscellaneous molecular pathology
  • Molecular genetics
  • Molecular pathology
  • MOLPATH
  • Nominal
  • PCR
  • Point in time
  • Random
  • Tissue
  • Tissue, unspecified
  • Variant Interpretation
  • WB
  • Whole blood
  • Whole blood or Tissue