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

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

LOINC status : TRIAL;

LOINC display name : Complex variant name Nom;

LOINC long common name : Complex variant name Nominal;

LOINC short name : Comp var name;

LOINC description : This term is used to report the formal name of a complex variant, including the reference sequence and details about the variation. For example, NM_000106.5(CYP2D6):c.[886C T;457G C] - Haplotype represents a CYP2D6 gene variant with haplotype nucleotide changes c.886C T and c.457G C and the NCBI reference sequence NM_000106.5. [http://www.ncbi.nlm.nih.gov/clinvar/variation/16895/];

Details

Origin ID

81261-0;

UMLS CUI

C4265553;

Has component
- Complex variant [LOINC component]
- Complex variant 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]
Semantic type(s)
- Clinical Attribute [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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