69547-8
LaboratoryGenomic ref allele [ID]
Definition
Reference values ("normal") examined within the Reference Sequence. This is used in a genotyping test to define the reference and variable nucleotide strings. That is if the sequence variation is an insertion, then Reference Nucleotide will be blank and Variable Nucleotide will contain the inserted nucleotides. In contrast, if the sequence variation is a deletion, then the Reference Nucleotide will contain the deleted nucliotieds, and the Variable Nucleotide will be blank.
LOINC 6-Axis Classification
Component
Reference nucleotide
Property
Prid
Time Aspect
Pt
System
Bld/Tiss
Scale Type
Nom
Method Type
Molgen
Details
Class
HL7.GENETICS
Order/Observation
Observation
Short Name
Ref nucleotide
Display Name
Reference nucleotide Molgen Nom (Bld/Tiss)
Related Names
Frequently Asked Questions
What is LOINC code 69547-8?
LOINC code 69547-8 identifies "Genomic ref allele [ID]". Reference values ("normal") examined within the Reference Sequence. This is used in a genotyping test to define the reference and variable nucleotide strings. That is if the sequence variation is an insertion, then Reference Nucleotide will be blank and Variable Nucleotide will contain the inserted nucleotides. In contrast, if the sequence variation is a deletion, then the Reference Nucleotide will contain the deleted nucliotieds, and the Variable Nucleotide will be blank.
What does 69547-8 measure?
This code measures Reference nucleotide in Bld/Tiss. It belongs to the HL7.GENETICS class in the LOINC classification.
What is LOINC?
LOINC (Logical Observation Identifiers Names and Codes) is a universal standard for identifying laboratory and clinical observations. It is maintained by the Regenstrief Institute and used worldwide for health data exchange.