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.

LOINCObservation

LOINC Code 83009-1: Genetic variation effect on high-risk allele Ql [Interp]

Name: LOINC Code 83009-1: Genetic variation effect on high-risk allele Ql [Interp]
Creator: HealthAssure Clinical Team
Published: 2026-05-21T09:00:10.305Z

83009-1 is a LOINC code used to identify Genetic variation effect on high-risk allele Ql [Interp] 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 variation effect on high-risk allele. It is commonly used with the system or sample type ^Patient.

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 variation effect on high-risk allele. It is commonly used with the system or sample type ^Patient.

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: TRIAL
Order vs observation: Observation

What it does not mean

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

Key facts

Genetic variation's effect on high-risk allele
Genetic variation effect on high-risk allele
Genetic var eff high-risk allele; Genetics; Genomic; Impression; Impression/interpretation of study; Impressions; Interp; Interpretation; Molecular pathology; MOLPATH; MOLPATH.PHARMG; Ordinal; Point in time; QL; Qual; Qualitative; Random; Screen

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 variation effect on high-risk allele Ql [Interp]Genetic variation's effect on high-risk alleleGenetic var eff high-risk alleleGenetic variation effect on high-risk alleleMOLPATH.PHARMGImpPt

Frequently asked questions

Code details

Code83009-1

SystemLOINC

Display nameGenetic variation effect on high-risk allele Ql [Interp]

DescriptionGenetic variation effect on high-risk allele

Short nameGenetic var eff high-risk allele

ComponentGenetic variation effect on high-risk allele

PropertyImp

TimingPt

System (specimen)^Patient

ScaleOrd

ClassMOLPATH.PHARMG

StatusTRIAL

Order/ObservationObservation

Flags

BillableNo

Valid clinical useNo

Source

SourceLOINC

Version2.82

Releasemain

First released2.58

Last changed2.73

Consumer names

Genetic variation effect on high-risk allele

Part names

Genetic variation effect on high-risk alleleImpPt^PatientOrdImpression/interpretation of studyPoint in time (spot)

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.