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 Name
LPA gene.c.3947+467T>C
Part Display Name
LPA gene.c.3947+467T>C
Part Type
Component (Describes the core component or analyte measured)
Created On
2019-04-24
Construct for LOINC Short Name
LPA c.3947+467T>C

LOINC Terminology Service (API) using HL7® FHIR® Get Info

CodeSystem lookup
https://fhir.loinc.org/CodeSystem/$lookup?system=http://loinc.org&code=LP343331-7

Language Variants Get Info

TagLanguageTranslation
zh-CNChinese (China)LPA 基因.c.3947+467T>C
it-ITItalian (Italy)LPA, gene.c.3947+467T>C
Synonyms: Gene LPA c.3947+467T>C
fr-FRFrench (France)LPA gène.c.3947+467T>C
es-ESSpanish (Spain)Gen LPA c.3947 + 467T> C
pl-PLPolish (Poland)LPA gen.c.3947+467T>C
Synonyms: Gen LPA c.3947+467T>C
el-GRGreek (Greece)Γονίδιο LPA.c.3947+467T>C
Synonyms: Γονίδιο LPA.c.3947+467T>C