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LOINC Code 94199-7: FGA gene full mutation analysis Sequencing Doc (Bld/Tiss)

94199-7 is a LOINC code used to identify FGA gene full mutation analysis Sequencing Doc (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 FGA gene full mutation analysis. 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 FGA gene full mutation analysis. 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: Both
  • Method: Sequencing

What it does not mean

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

Key facts

FGA gene full mutation analysis in Blood or Tissue by Sequencing
FGA gene full mutation analysis
Full gene sequence analysis is performed to test for the presence of a mutation in the coding regions and intron/exon boundaries of the fibrinogen alpha chain (FGA) gene. Mutations in the FGA gene are associated with congenital afibrinogenemia (also hypofibrinogenemia, dysfibrinogenemia, or hypodysfibrinogenemia) and familial renal amyloidosis.[GHR geneFGA]
Blood; Document; Fib2; fibrinogen alpha chain; Finding; Findings; full gene sequencing; Full Mut Anl; Genetics; Heredity; Heritable; high-throughput sequencing; HTS; Inherited; Molecular pathology; MOLPATH; Mut; Mutations; Next generation sequencing; NGS; Point in time; Random; sequencing of entire coding region; Tissue; Tissue, unspecified; 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

FGA gene full mutation analysis Sequencing Doc (Bld/Tiss)FGA gene full mutation analysis in Blood or Tissue by SequencingFGA Full Mut Anl Bld/T SeqFGA gene full mutation analysisMOLPATHFGA gene variant analysis, Blood or tissue specimenFind

Frequently asked questions

Code details

Code94199-7
SystemLOINC
Display nameFGA gene full mutation analysis Sequencing Doc (Bld/Tiss)
DescriptionFGA gene full mutation analysis
Short nameFGA Full Mut Anl Bld/T Seq
ComponentFGA gene full mutation analysis
PropertyFind
TimingPt
System (specimen)Bld/Tiss
ScaleDoc
MethodSequencing
ClassMOLPATH
StatusACTIVE
Order/ObservationBoth

Flags

BillableNo
Valid clinical useNo

Source

SourceLOINC
Version2.82
Releasemain
First released2.68
Last changed2.68

Consumer names

FGA gene variant analysis, Blood or tissue specimen

Part names

FGA gene full mutation analysisFindPtBld/TissDocSequencingFindingPoint in time (spot)Blood or Tissue

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.