LOINC
Version 2.71

81262-8Complex variant HGVS nameTrial

Status Information

Status
Trial

Term Description

This 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.
Source: Regenstrief LOINC

Fully-Specified Name

Component
Complex variant HGVS name
Property
Find
Time
Pt
System
^Patient
Scale
Nom
Method

Additional Names

Short Name
Comp var HGVS name
Display Name
Complex variant HGVS name Nom
Consumer Name Alpha
Complex Variant HGVS Name

Basic Attributes

Class
MOLPATH
Type
Laboratory
First Released
Version 2.56
Last Updated
Version 2.56
Order vs. Observation
Observation

Member of these Panels

LOINC Long Common Name
81247-9 Master HL7 genetic variant reporting panel

Language Variants Get Info

zh-CNChinese (China)
复杂变异 HGVS 命名:发现:时间点:^患者:名义型:
fr-FRFrench (France)
Variant complexe HGVS nom:Recherche:Ponctuel:Patient:Résultat nominal:
it-ITItalian (Italy)
Variante complessa nome HGVS:Osservazione:Pt:^Paziente:Nom:
es-ESSpanish (Spain)
Nombre de la variante compleja HGVS:Hallazgo:Punto temporal:^paciente:Nom:

LOINC FHIR® API Example - CodeSystem Request Get Info

https://fhir.loinc.org/CodeSystem/$lookup?system=http://loinc.org&code=81262-8