Genetics results LP70194-3

LOINC Hierarchy

LOINC part code	LP70194-3
name	Genetics results
type	COMPONENT
status	ACTIVE
children	LOINC Home {component} LP432695-7 Laboratory LP29693-6 Molecular pathology LP7822-2 Genetics results LP70194-3 ▸ 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

Copyright © 2026 Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright © 1995-2026, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee. See https://loinc.org/license for the full LOINC copyright and license.

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LOINC Home

{component} LP432695-7

Laboratory LP29693-6

Molecular pathology LP7822-2

Genetics results LP70194-3

LOINC Hierarchy

▸ 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