OMOP Concept 37041864
Simple variant panel | Patient | Molecular Pathology Panels
ClassificationMeasurementLOINCLP401935-4LOINC Hierarchy
Maps from
0
Descendants
28
Valid from
1 Jan 1970
Valid to
31 Dec 2099
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Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(4)Roll up to these when you need a wider cohort.
Narrower concepts
(28)Included automatically when you query with descendants.
- 1Discrete genetic variant panel
- 2Allelic phase
- 2Allelic read depth
- 2Allelic state
- 2Amino acid change (pHGVS)
- 2Amino acid change [Type]
- 2Associated phenotype
- 2Basis for allelic phase [Type]
- 2CIGAR [ID]
- 2Cytogenetic (chromosome) location
- 2dbSNP [ID]
- 2Discrete genetic variant
- 2DNA change (c.HGVS)
- 2DNA change type
- 2Gene studied [ID]
- 2Genetic variant assessment
- 2Genetic variation clinical significance [Imp]
- 2Genomic allele start-end
- 2Genomic alt allele [ID]
- 2Genomic DNA change (gHGVS)
- 2Genomic ref allele [ID]
- 2Genomic reference sequence [ID]
- 2Genomic source class [Type]
- 2Haplotype name
- 2Sample variant allelic frequency [NFr]
- 2Transcript reference sequence [ID]
- 2Variant analysis method [Type]
- 2Variant category
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