OMOP Concept 37053635
Complex variant panel | Patient | Molecular Pathology Panels
ClassificationMeasurementLOINCLP401913-1LOINC Hierarchy
Maps from
0
Descendants
32
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
(32)Included automatically when you query with descendants.
- 1Complex genetic variant panel
- 2Allelic state
- 2Associated phenotype
- 2Basis for allelic phase [Type]
- 2Complex genetic variant [ID]
- 2Complex variant HGVS name
- 2Complex variant type
- 2Discrete genetic variant panel
- 2Genetic variation clinical significance [Imp]
- 3Allelic phase
- 3Allelic read depth
- 3Amino acid change (pHGVS)
- 3Amino acid change [Type]
- 3CIGAR [ID]
- 3Cytogenetic (chromosome) location
- 3dbSNP [ID]
- 3Discrete genetic variant
- 3DNA change (c.HGVS)
- 3DNA change type
- 3Gene studied [ID]
- 3Genetic variant assessment
- 3Genomic allele start-end
- 3Genomic alt allele [ID]
- 3Genomic DNA change (gHGVS)
- 3Genomic ref allele [ID]
- 3Genomic reference sequence [ID]
- 3Genomic source class [Type]
- 3Haplotype name
- 3Sample variant allelic frequency [NFr]
- 3Transcript reference sequence [ID]
- 3Variant analysis method [Type]
- 3Variant category
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