94716-8
LOINC Code
| LOINC code | 94716-8 | |
|---|---|---|
| name | ||
| description | 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] | |
| status | ACTIVE | |
Fully-Specified Name | ||
| component | AGTR1 gene.c.1166A>C | |
| property | Geno = Genotype | |
| time | Pt = Point in time: To identify measures at a point in time. This is a synonym for “spot” or “random” as applied to urine measurements. | |
| system | Bld = Whole blood | |
| scale | Nom = Nominal: Nominal or categorical responses that do not have a natural ordering. (e.g., names of bacteria, reported as answers, categories of appearance that do not have a natural ordering, such as, yellow, clear, bloody. | |
| method | Molgen = Molecular Genetics: General class of methods used to detect genetic attributes on a molecular basis including RFL, PCR and other methods. | |
Additional Names | ||
| short name | 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 | |
Basic Attributes | ||
| class | MOLPATH.MUT | |
| type | 1 Laboratory | |
| order vs. observation | AGTR1 c.1166A>C | |
History/Usage | ||
| first released | ||
| last updated | 2.68 | |
| last change type | ADD - added | |
Related Names | ||
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