94716-8

LOINC 2.82

AGTR1 gene c.1166A>C [Genotype] in Blood by Molecular genetics method Nominal

AGTR1 c.1166A>C Geno Bld

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]

Component

  • AGTR1 gene.c.1166A>C

Specimen / system

  • Bld

Class

  • MOLPATH.MUT

Property

  • Geno

Scale

  • Nom

Method

  • Molgen

Related names

  • AGTR1 c.1166A>C; Blood; Genetics; Heredity; Heritable; Inherited; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Nominal; PCR; Point in time; Random; WB; Whole blood

Index terms

  • AGTR1 c.1166A&gt
  • AGTR1 gene.c.1166A>C
  • Blood
  • C
  • Genetics
  • Heredity
  • Heritable
  • Inherited
  • Molecular genetics
  • Molecular pathology
  • MOLPATH
  • MOLPATH.MUTATIONS
  • Nominal
  • PCR
  • Point in time
  • Random
  • WB
  • Whole blood