LOINCActiveBoth

LOINC Code 95555-9: F7 gene p.Arg353Gln genotype Molgen (Bld/Tiss)

95555-9 is a LOINC code used to identify F7 gene p.Arg353Gln genotype Molgen (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 F7 gene.p.Arg353Gln. 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 F7 gene.p.Arg353Gln. 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: Molgen

What it does not mean

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

Key facts

  • F7 gene p.Arg353Gln [Genotype] in Blood or Tissue by Molecular genetics method Nominal
  • F7 gene.p.Arg353Gln
  • Detection of the polymorphism variant R353Q (p.Arg353Gln, rs6046) in the Factor VII gene that may confer protection against thrombosis.
  • Blood; CF gene; coagulation factor VII (serum prothrombin conversion accelerator); Coagulation factor VII gene; F7 R353Q; Factor 7; Factor VII; Factor VII Deficiencies; Genetics; Heredity; Heritable; Inherited; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Nominal; P prime; PCR; Point in time; Random; rs6046; Serum prothrombin conversion accelerator; SPCA; Thrombophilia; 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

F7 gene p.Arg353Gln genotype Molgen (Bld/Tiss)F7 gene p.Arg353Gln [Genotype] in Blood or Tissue by Molecular genetics method NominalF7 R353Q Geno Bld/TF7 gene.p.Arg353GlnMOLPATH.MUTF7 gene p.Arg353Gln genotype, Blood or tissue specimenGeno

Frequently asked questions

Code details

Code95555-9
SystemLOINC
Display nameF7 gene p.Arg353Gln genotype Molgen (Bld/Tiss)
DescriptionF7 gene.p.Arg353Gln
Short nameF7 R353Q Geno Bld/T
ComponentF7 gene.p.Arg353Gln
PropertyGeno
TimingPt
System (specimen)Bld/Tiss
ScaleNom
MethodMolgen
ClassMOLPATH.MUT
StatusACTIVE
Order/ObservationBoth

Flags

BillableNo
Valid clinical useNo

Source

SourceLOINC
Version2.82
Releasemain
First released2.69
Last changed2.69

Consumer names

F7 gene p.Arg353Gln genotype, Blood or tissue specimen

Part names

F7 gene.p.Arg353GlnGenoPtBld/TissNomMolgenF7 gene p.Arg353GlnGenotypePoint 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.