81262-8

LOINC Code


LOINC code81262-8
name
descriptionThis term is used to report the name of the complex variant found in this study in HGVS format. For example, c.[886C>T;457G>C], which represents two separate base substitutions in one gene on one chromosome, or c.[886C>T];[457G>C], which represents two separate base substitutions in one gene on two different chromosomes.
statusTRIAL

Fully-Specified Name

componentComplex variant HGVS name
propertyFind  =  Finding
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
scaleNom  =  Nominal:  Nominal or categorical responses that do not have a natural ordering. (e.g., names of bacteria, reported as answers, categories of appearance that do not have a natural ordering, such as, yellow, clear, bloody.
method

Additional Names

short nameComp var; Comp var HGVS name; Compx; Finding; Findings; Molecular pathology; MOLPATH; Nominal; Point in time; Random

Basic Attributes

classMOLPATH
type1  Laboratory
order vs. observationComp var HGVS n

Member of these Panels

81251-1

History/Usage

first released
last updated2.56
last change typeADD  - added

Related Names



Copyright © 2026 Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright © 1995-2026, 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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