94716-8
LaboratoryAGTR1 gene c.1166A>C [Genotype] in Blood by Molecular genetics method Nominal
Definition
The patient's genotype for the c.1166A>C (rs5186) variant in the AGTR1 (angiotensin II receptor type 1) gene. Presence of the C allele is associated with and increased risk of hypertension and cardiovascular risk.[PMID: 20703234]
LOINC 6-Axis Classification
Component
AGTR1 gene.c.1166A>C
Property
Geno
Time Aspect
Pt
System
Bld
Scale Type
Nom
Method Type
Molgen
Details
Class
MOLPATH.MUT
Order/Observation
Both
Short Name
AGTR1 c.1166A>C Geno Bld
Display Name
AGTR1 gene c.1166A>C genotype Molgen (Bld)
Related Names
Frequently Asked Questions
What is LOINC code 94716-8?
LOINC code 94716-8 identifies "AGTR1 gene c.1166A>C [Genotype] in Blood by Molecular genetics method Nominal". The patient's genotype for the c.1166A>C (rs5186) variant in the AGTR1 (angiotensin II receptor type 1) gene. Presence of the C allele is associated with and increased risk of hypertension and cardiovascular risk.[PMID: 20703234]
What does 94716-8 measure?
This code measures AGTR1 gene.c.1166A>C in Bld. It belongs to the MOLPATH.MUT 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.