Complex genetic variant panel   81251-1

LOINC Code


LOINC code81251-1
nameComplex genetic variant panel
descriptionThis panel is used to report information related to a complex genetic variant and includes a repeating subpanel for reporting specific information for each simple variation that the complex variant includes.
statusTRIAL

Fully-Specified Name

componentComplex variant panel
property-
timePt  =  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^Patient
scale-
method

Additional Names

short nameComp var pnl

Basic Attributes

classPANEL.MOLPATH
type1  Laboratory
order vs. observationOrder

Panel Components

81260-2Complex genetic variant [ID]
81262-8Complex variant HGVS name
81263-6Complex variant type
81259-4Associated phenotype
53037-8Genetic variation clinical significance [Imp]
53034-5Allelic state
82309-6Basis for allelic phase [Type]
81250-3Discrete genetic variant panel

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.

Member of these Panels

81247-9Master HL7 genetic variant reporting panel

History/Usage

first released
last updated2.58
last change typeMIN  - change to field other than name

Related Names

Comp var
Comp var pnl
Compx
Molecular pathology
MOLPATH
Pan
Panel.molpath
Panl
Pnl
Point in time
Random

Copyright © 2024 Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright © 1995-2024, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee. See https://loinc.org/license for the full LOINC copyright and license.

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