HTR2A c.614-20502G>C

Variant ID: 13-47430276-C-G

NM_000621.4(HTR2A):c.614-20502G>C

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.

The Pharmacogenomics Journal
Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL
Publication Date: 2019-04

Variant appearance in text: rs1885884
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Genetics of suicide attempts in individuals with and without mental disorders: a population-based genome-wide association study.

Molecular Psychiatry
Erlangsen, Annette A; Appadurai, Vivek V; Wang, Yunpeng Y; Turecki, Gustavo G; Mors, Ole O; Werge, Thomas T; Mortensen, Preben B PB; Starnawska, Anna A; Børglum, Anders D AD; Schork, Andrew A; Nudel, Ron R; Bækvad-Hansen, Marie M; Bybjerg-Grauholm, Jonas J; Hougaard, David M DM; Thompson, Wesley K WK; Nordentoft, Merete M; Agerbo, Esben E
Publication Date: 2020-10

Variant appearance in text: rs1885884
PubMed Link: 30116032
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic Association Studies of Suicidal Behavior: A Review of the Past 10 Years, Progress, Limitations, and Future Directions.

Frontiers In Psychiatry
Mirkovic, Bojan B; Laurent, Claudine C; Podlipski, Marc-Antoine MA; Frebourg, Thierry T; Cohen, David D; Gerardin, Priscille P
Publication Date: 2016

Variant appearance in text: rs1885884
PubMed Link: 27721799
Variant Present in the following documents:
  • Main text
  • fpsyt-07-00158.pdf
View BVdb publication page