Genetic variant details in Blood or Tissue by Molecular genetics method Narrative 82939-0
LOINC Code
LOINC code | 82939-0 | ||
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name | Genetic variant details in Blood or Tissue by Molecular genetics method Narrative | ||
description | 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). | ||
status | ACTIVE | ||
Fully-Specified Name | |||
component | Genetic variant details | ||
property | Find = Finding | ||
time | Pt = Point in time: To identify measures at a point in time. This is a synonym for “spot” or “random” as applied to urine measurements. | ||
system | Bld/Tiss Bld = Whole blood Tiss = Tissue, unspecified | ||
scale | Nar = Narrative: Text narrative, such as the description of a microscopic part of a surgical papule test. | ||
method | Molgen = Molecular Genetics: General class of methods used to detect genetic attributes on a molecular basis including RFL, PCR and other methods. | ||
Additional Names | |||
short name | Genetic variant details Bld/T | ||
Basic Attributes | |||
class | MOLPATH | ||
type | 1 Laboratory | ||
order vs. observation | Both | ||
Associated Observations | |||
LOINC codes that represent optional associated observation(s) for a clinical observation or laboratory test. A LOINC term may represent a single associated observation or panel containing several associated observations. | |||
History/Usage | |||
test rank | 6121 of 2000 most commonly performed tests by labs in USA | ||
first released | |||
last updated | 2.73 | ||
last change type | MIN - change to field other than name | ||
Related Names | |||
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