Complex variant HGVS name:Find:Pt: Patient:Nom:

Preferred Label : Complex variant HGVS name:Find:Pt: Patient:Nom:;

LOINC status : TRIAL;

LOINC display name : Complex variant HGVS name Nom;

LOINC long common name : Complex variant HGVS name;

LOINC short name : Comp var HGVS name;

LOINC 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.;

Details

Origin ID

81262-8;

UMLS CUI

C4255286;

Has component
- Complex variant [LOINC component]
- Complex variant HGVS name [LOINC component]
- Name [LOINC component]
Has property
- Finding [LOINC Property]
Has scale
- Nom [LOINC scale]
Has system
- Patient [LOINC System]
- ^Patient [LOINC System]
Has time aspect
- Point in time (spot) [LOINC time aspect]
Part of panel
- Complex variant panel:-:Pt:^Patient:-: [LOINC code]
Semantic type(s)
- Clinical Attribute [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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