82939-0
LaboratoryGenetic variant details in Blood or Tissue by Molecular genetics method Narrative
Definition
Narrative information (unstructured) about a genetic variant. The results may state that a mutation was not identified or include the variant(s) found. The location of the variant may be described at various levels, such as genomic (g.), coding (c.), and protein (p.) levels. Details may also include alternate identifiers for the variant (e.g dbSNP ID, Transcript reference sequence ID), the clinical significance (e.g. pathogenic, variant of unknown significance) and the change type (e.g. homozygous, heterozygous, wild type).
LOINC 6-Axis Classification
Component
Genetic variant details
Property
Find
Time Aspect
Pt
System
Bld/Tiss
Scale Type
Nar
Method Type
Molgen
Details
Class
MOLPATH
Order/Observation
Both
Short Name
Genetic variant details Bld/T
Display Name
Genetic variant details Molgen Nar (Bld/Tiss)
Related Names
Frequently Asked Questions
What is LOINC code 82939-0?
LOINC code 82939-0 identifies "Genetic variant details in Blood or Tissue by Molecular genetics method Narrative". Narrative information (unstructured) about a genetic variant. The results may state that a mutation was not identified or include the variant(s) found. The location of the variant may be described at various levels, such as genomic (g.), coding (c.), and protein (p.) levels. Details may also include alternate identifiers for the variant (e.g dbSNP ID, Transcript reference sequence ID), the clinical significance (e.g. pathogenic, variant of unknown significance) and the change type (e.g. homozygous, heterozygous, wild type).
What does 82939-0 measure?
This code measures Genetic variant details in Bld/Tiss. It belongs to the MOLPATH class in the LOINC classification.
What is LOINC?
LOINC (Logical Observation Identifiers Names and Codes) is a universal standard for identifying laboratory and clinical observations. It is maintained by the Regenstrief Institute and used worldwide for health data exchange.