KCNH2 c.307+585G>T

Variant ID: 7-150671214-C-A

NM_000238.3(KCNH2):c.307+585G>T

This variant was identified in 7 publications

View GRCh38 version.




Publications:


Analysis of CACNA1C and KCNH2 Risk Variants on Cardiac Autonomic Function in Patients with Schizophrenia.

Genes
Refisch, Alexander A; Komatsuzaki, Shoko S; Ungelenk, Martin M; Schumann, Andy A; Chung, Ha-Yeun HY; Schilling, Susann S SS; Jantzen, Wibke W; Schröder, Sabine S; Nöthen, Markus M MM; Mühleisen, Thomas W TW; Hübner, Christian A CA; Bär, Karl-Jürgen KJ
Publication Date: 2022-11-16

Variant appearance in text: rs3800779
PubMed Link: 36421807
Variant Present in the following documents:
  • Main text
  • genes-13-02132.pdf
View BVdb publication page



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: rs3800779
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



GWAS of 89,283 individuals identifies genetic variants associated with self-reporting of being a morning person.

Nature Communications
Hu, Youna Y; Shmygelska, Alena A; Tran, David D; Eriksson, Nicholas N; Tung, Joyce Y JY; Hinds, David A DA
Publication Date: 2016-02-02

Variant appearance in text: rs3800779
PubMed Link: 26835600
Variant Present in the following documents:
  • Main text
  • ncomms10448.pdf
View BVdb publication page



Association between polymorphisms in NOS3 and KCNH2 and social memory.

Frontiers In Neuroscience
Henningsson, Susanne S; Zettergren, Anna A; Hovey, Daniel D; Jonsson, Lina L; Svärd, Joakim J; Cortes, Diana S DS; Melke, Jonas J; Ebner, Natalie C NC; Laukka, Petri P; Fischer, Håkan H; Westberg, Lars L
Publication Date: 2015

Variant appearance in text: rs3800779
PubMed Link: 26539080
Variant Present in the following documents:
  • Main text
  • fnins-09-00393.pdf
View BVdb publication page



Personalized medicine in psychiatry: problems and promises.

Bmc Medicine
Ozomaro, Uzoezi U; Wahlestedt, Claes C; Nemeroff, Charles B CB
Publication Date: 2013-05-16

Variant appearance in text: rs3800779
PubMed Link: 23680237
Variant Present in the following documents:
  • Main text
  • 1741-7015-11-132.pdf
View BVdb publication page



Major channels involved in neuropsychiatric disorders and therapeutic perspectives.

Frontiers In Genetics
Imbrici, Paola P; Camerino, Diana Conte DC; Tricarico, Domenico D
Publication Date: 2013

Variant appearance in text: rs3800779
PubMed Link: 23675382
Variant Present in the following documents:
  • Main text
View BVdb publication page



Two four-marker haplotypes on 7q36.1 region indicate that the potassium channel gene HERG1 (KCNH2, Kv11.1) is related to schizophrenia: a case control study.

Behavioral And Brain Functions : Bbf
Atalar, Fatmahan F; Acuner, Tufan Tevfik TT; Cine, Naci N; Oncu, Fatih F; Yesilbursa, Dogan D; Ozbek, Ugur U; Turkcan, Solmaz S
Publication Date: 2010-05-28

Variant appearance in text: HERG: 307+585G>T; rs3800779
PubMed Link: 20507645
Variant Present in the following documents:
  • Main text
  • 1744-9081-6-27.pdf
View BVdb publication page