OMOP Concept 37033495
Sequence variation panel | Blood or Tissue | Molecular Pathology Panels
ClassificationMeasurementLOINCLP401933-9LOINC Hierarchy
Maps from
0
Descendants
14
Valid from
1 Jan 1970
Valid to
31 Dec 2099
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Broader concepts
(4)Roll up to these when you need a wider cohort.
Narrower concepts
(14)Included automatically when you query with descendants.
- 1Sequence variation panel - Blood or Tissue by Molecular genetics method
- 2Amino acid change (pHGVS)
- 2Amino acid change [Type]
- 2Chromosome [Identifier] in Blood or Tissue by Molecular genetics method
- 2Cytogenetic (chromosome) location
- 2DNA change (c.HGVS)
- 2DNA change type
- 2DNA region name [Identifier]
- 2DNA sequence variation display name [Text] Narrative
- 2DNA sequence variation identifier [Identifier]
- 2Gene studied [ID]
- 2Genetic variant allelic state [Type] in Blood or Tissue by Molecular genetics method
- 2Genetic variant clinical significance [Interpretation] in Blood or Tissue by Molecular genetics method
- 2Genomic source class [Type]
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