Genetics results LP70194-3
LOINC Hierarchy
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▸ HL7 genetics LP70593-6
▸ HL7 cytogenetics LP111381-2
▸ Allelic frequency LP212300-0
▸ Allelic phase LP213621-8
▸ Allelic read depth LP213622-6
▸ Associated phenotype LP212301-8
▸ Basis for allelic phase LP220487-5
▸ Cells with cytogenetic abnormality LP410953-6
▸ Clinical cytogeneticist LP62867-4
▸ Chromosome painting analysis LP208607-4
▸ CIGAR LP212299-4
▸ ClinVar version LP232210-7
▸ Complex variant LP212306-7
▸ COSMIC simple variant LP213614-3
▸ COSMIC structural variant LP213615-0
▸ COSMIC version LP232209-9
▸ dbSNP LP212297-8
▸ dbSNP version LP213616-8
▸ Default genomic reference sequence coding system LP212292-9
▸ Default transcript reference sequence coding system LP217243-7
▸ Gene fusion transcript details LP418370-5
▸ Gene studied with no variant found LP411464-3
▸ Genetic diseases LP62869-0
▸ Genetic form configuration controls LP212393-5
▸ Genetic variant details LP232001-0
▸ Variant exact start-end LP212296-0
▸ Genomic coordinate system LP343929-8
▸ Genomic structural variant copy number LP213662-2
▸ Genomic structural variant name LP213661-4
▸ Genotype display name LP234803-7
▸ Haplotype name LP234797-1
▸ HGVS version LP212399-2
▸ Level of evidence LP345149-1
▸ Nuclei scored LP113318-2
▸ Origin of germline genetic variant LP417220-3
▸ Precision of boundaries LP212319-0
▸ Primer set LP438600-1
▸ Range(s) of DNA sequences examined LP212392-7
▸ Sample variant allelic frequency LP343831-6
▸ Simple variant LP212295-2
▸ Source of population allelic frequency data LP343958-7
▸ Structural variant LP212310-9
▸ Variant category LP232211-5
▸ Variant coding system LP213620-0
▸ Variant of unknown significance LP411465-0
▸ Vendor FISH product name LP199189-4
▸ Whole exome sequence analysis LP248469-1
▸ Whole genome sequence analysis LP248470-9
▸ Whole mRNA transcriptome sequence analysis LP417648-5
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