LP343317-6
LPA gene.c.5673A>G
Active
Description
The LPA gene, previously called LP, is located on chromosome 6 and encodes the apolipoprotein(a) portion of lipoprotein(a) [Lp(a)]. Several variants in the LPA gene have been associated with increased levels of Lp(a) as well as increased risk of cardiovascular disease. One of these variants is c.5673A>G (rs3798220), which results in a change from isoleucine to methionine at position 4399 (p.Ile4399Met, also known previously as position 1891). Another variant is c.3947+467T>C (rs10455872), which is located in intron 25. PMID: 27605514 Source: Regenstrief LOINC
Basic Part Properties
- Part Display Name
- LPA gene.c.5673A>G
- Part Type
- Component (Describes the core component or analyte measured)
- Created On
- 2019-04-24
- Construct for LOINC Short Name
- LPA c.5673A>G
LOINC Terminology Service (API) using HL7® FHIR® Get Info
Requests to this service require a free LOINC username and password. Below is a sample of the possible capabilities. See the LOINC Terminology Service documentation for more information.
- CodeSystem lookup
- https:
//fhir.loinc.org/CodeSystem/$lookup?system=http: //loinc.org&code=LP343317-6
Language Variants Get Info
| Tag | Language | Translation |
|---|---|---|
| zh-CN | Chinese (China) | LPA 基因.c.5673A>G |
| it-IT | Italian (Italy) | LPA, gene.c.5673A>G Synonyms: Gene LPA c.5673A>G |
| es-ES | Spanish (Spain) | Gen LPA c.5673A> G |
LOINC Copyright
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