KCNH2 c.308-377T>G

Variant ID: 7-150657201-A-C

NM_000238.3(KCNH2):c.308-377T>G

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Association of FAAH p.Pro129Thr and COMT p.Ala72Ser with schizophrenia and comorbid substance use through next-generation sequencing: an exploratory analysis.

Revista Brasileira De Psiquiatria (Sao Paulo, Brazil : 1999)
Martínez-Magaña, José J JJ; Genis-Mendoza, Alma D AD; González-Covarrubias, Vanessa V; Juárez-Rojop, Isela E IE; Tovilla-Zárate, Carlos A CA; Soberón, Xavier X; Lanzagorta, Nuria N; Nicolini, Humberto H
Publication Date: 2022

Variant appearance in text: rs12668582
PubMed Link: 34037083
Variant Present in the following documents:
  • bjp-44-02-164.pdf
View BVdb publication page



The contribution of non-coding regulatory elements to cardiovascular disease.

Open Biology
Villar, Diego D; Frost, Stephanie S; Deloukas, Panos P; Tinker, Andrew A
Publication Date: 2020-07

Variant appearance in text: rs12668582
PubMed Link: 32603637
Variant Present in the following documents:
  • rsob-10-200088.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: rs12668582
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page