" /> Complex variant:ID:Pt: Patient:Nom: - CISMeF





Preferred Label : Complex variant:ID:Pt: Patient:Nom:;

LOINC status : TRIAL;

LOINC display name : Complex variant Nom [ID];

LOINC long common name : Complex genetic variant [ID];

LOINC short name : Comp var ID;

LOINC description : This term is used to report the unique identifier of the complex variant found in this study. The identifier may come from various sources, including NCBI's ClinVar and Ensembl. For example, the variant NM_000106.5(CYP2D6):c.[886C T;457G C] - Haplotype has the ClinVar ID 16895. [http://www.ncbi.nlm.nih.gov/clinvar/variation/16895/];

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27/07/2025


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