Description

The rs7997012 (c.614-2211T>C) variant is located in intron 2 of the HTR2A gene and codes for the 5-HT2A serotonin receptor. The variant has been identified as a marker of citalopram response. Patients with depression who are genotype AA are associated with increased likelihood of response when treated with citalopram as compared to genotype GG.[NCBI ClinVar ID: RCV000211197][OMIM: 182135#0003] Source: Regenstrief LOINC

Basic Part Properties

Part Name
HTR2A gene.c.614-2211T>C
Part Display Name
HTR2A gene c.614-2211T>C
Part Type
Component (Describes the core component or analyte measured)
Created On
2019-07-25
Construct for LOINC Short Name
HTR2A c.614-2211T>C

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

CodeSystem lookup
https://fhir.loinc.org/CodeSystem/$lookup?system=http://loinc.org&code=LP411023-7

Language Variants Get Info

TagLanguageTranslation
zh-CNChinese (China)HTR2A 基因.c.614-2211T>C
it-ITItalian (Italy)HTR2A, gene.c.614-2211T>C
Synonyms: Gene HTR2A c.614-2211T>C
fr-FRFrench (France)HTR2A gène mutation c.614-2211T>C
es-ESSpanish (Spain)Gen HTR2A c.614-2211T> C
pl-PLPolish (Poland)HTR2A gen.c.614-2211T>C
Synonyms: Gen HTR2A c.614-2211T>C
el-GRGreek (Greece)Γονίδιο HTR2A c.614-2211T>C
Synonyms: Γονίδιο HTR2A c.614-2211T>C