LOINC display name : Genetic variant details Molgen Nar (Bld/Tiss);
LOINC long common name : Genetic variant details in Blood or Tissue by Molecular genetics method Narrative;
LOINC short name : Genetic variant details Bld/T;
LOINC description : Narrative information (unstructured) about a genetic variant. The results may state
that a mutation was not identified or include the variant(s) found. The location of
the variant may be described at various levels, such as genomic (g.), coding (c.),
and protein (p.) levels. Details may also include alternate identifiers for the variant
(e.g dbSNP ID, Transcript reference sequence ID), the clinical significance (e.g.
pathogenic, variant of unknown significance) and the change type (e.g. homozygous,
heterozygous, wild type).;
Has component