What does this LOINC code represent?

This LOINC code identifies a lab observation, measurement, question, or clinical concept in a standardized format.

Is this enough to understand my test result?

No. The code identifies the test or observation, but the interpretation depends on the actual result, reference range, and clinical context.

LOINCActiveObservation

LOINC Code 48007-9: Genetic variant allelic state Molgen Nom (Bld/Tiss)

Name: LOINC Code 48007-9: Genetic variant allelic state Molgen Nom (Bld/Tiss)
Creator: HealthAssure Clinical Team
Published: 2026-05-21T08:59:32.262Z

48007-9 is a LOINC code used to identify Genetic variant allelic state Molgen Nom (Bld/Tiss) in laboratory and clinical observation data. You may see this code in lab systems, lab reports, EHR exports, interoperability feeds, or other structured clinical data exchanges. LOINC codes identify tests, measurements, observations, survey items, and clinical questions in a standardized way. It is associated with the component Genetic variant allelic state. It is commonly used with the system or sample type Bld/Tiss.

Reviewed by HealthAssure Clinical TeamUpdated 21 May 2026

What is this code?

LOINC codes identify tests, measurements, observations, survey items, and clinical questions in a standardized way. It is associated with the component Genetic variant allelic state. It is commonly used with the system or sample type Bld/Tiss.

When is it used?

Used in lab systems, EHRs, and clinical data exchange.
May identify a test, observation, survey item, or clinical document request rather than a diagnosis.
Status: ACTIVE
Order vs observation: Observation
Method: Molgen

What it does not mean

The code identifies the observation or test, not the actual result.

Key facts

Genetic variant allelic state [Type] in Blood or Tissue by Molecular genetics method

Genetic variant allelic state

Example answer1^Heteroplasmic ^LA Definition: When information about the state of each of the paired genes is important (e.g. because it may only have an effect if homozygous) - report that information here

Blood; Genetics; Genomic; MISC; Miscellaneous molecular pathology; Molecular genetics; Molecular pathology; MOLPATH; Nominal; PCR; Point in time; Random; Tissue; Tissue, unspecified; Typ; WB; Whole blood; Whole blood or Tissue

Where you may see this code

You may see this code in lab systems, lab reports, EHR exports, interoperability feeds, or other structured clinical data exchanges.

Common synonyms

Genetic variant allelic state Molgen Nom (Bld/Tiss)Genetic variant allelic state [Type] in Blood or Tissue by Molecular genetics methodGenetic variant allelic state Bld/TGenetic variant allelic stateMOLPATH.MISCGenetic variant allelic state, Blood or tissue specimenType

Frequently asked questions

Code details

Code48007-9

SystemLOINC

Display nameGenetic variant allelic state Molgen Nom (Bld/Tiss)

DescriptionGenetic variant allelic state

Short nameGenetic variant allelic state Bld/T

ComponentGenetic variant allelic state

PropertyType

TimingPt

System (specimen)Bld/Tiss

ScaleNom

MethodMolgen

ClassMOLPATH.MISC

StatusACTIVE

Order/ObservationObservation

Flags

BillableNo

Valid clinical useNo

Source

SourceLOINC

Version2.82

Releasemain

First released2.21

Last changed2.26

Consumer names

Genetic variant allelic state, Blood or tissue specimen

Part names

Genetic variant allelic stateTypePtBld/TissNomMolgenPoint in time (spot)Blood or TissueMolecular genetics

About this content

This page is prepared by HealthAssure's clinical team using official coding standards from LOINC. AI tools assist with drafting explanations, which are then reviewed and verified by healthcare professionals for accuracy. This content is for informational purposes and does not replace professional medical advice. Meet our team.