NOS1AP c.106-16076A>G

Variant ID: 1-162108119-A-G

NM_014697.2(NOS1AP):c.106-16076A>G

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Associations between NOS1AP single nucleotide polymorphisms (SNPs) and QT interval duration in four racial/ethnic groups in the Multi-Ethnic Study of Atherosclerosis (MESA).

Annals Of Noninvasive Electrocardiology : The Official Journal Of The International Society For Holter And Noninvasive Electrocardiology, Inc
Shah, Sidharth A SA; Herrington, David M DM; Howard, Timothy D TD; Divers, Jasmin J; Arnett, Donna K DK; Burke, Greg L GL; Kao, Weng Hong WH; Guo, Xiuqing X; Siscovick, David S DS; Chakravarti, Aravinda A; Lima, Joao A JA; Psaty, Bruce M BM; Tomaselli, Gordon F GF; Rich, Stephen S SS; Bowden, Donald W DW; Post, Wendy W
Publication Date: 2013-01

Variant appearance in text: rs4657154
PubMed Link: 23347024
Variant Present in the following documents:
  • Main text
View BVdb publication page



NOS1AP variant associated with incidence of type 2 diabetes in calcium channel blocker users in the Atherosclerosis Risk in Communities (ARIC) study.

Diabetologia
Chu, A Y AY; Coresh, J J; Arking, D E DE; Pankow, J S JS; Tomaselli, G F GF; Chakravarti, A A; Post, W S WS; Spooner, P H PH; Boerwinkle, E E; Kao, W H L WH
Publication Date: 2010-03

Variant appearance in text: rs4657154
PubMed Link: 19943157
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic variations in nitric oxide synthase 1 adaptor protein are associated with sudden cardiac death in US white community-based populations.

Circulation
Kao, W H Linda WH; Arking, Dan E DE; Post, Wendy W; Rea, Thomas D TD; Sotoodehnia, Nona N; Prineas, Ronald J RJ; Bishe, Bryan B; Doan, Betty Q BQ; Boerwinkle, Eric E; Psaty, Bruce M BM; Tomaselli, Gordon F GF; Coresh, Josef J; Siscovick, David S DS; Marbán, Eduardo E; Spooner, Peter M PM; Burke, Gregory L GL; Chakravarti, Aravinda A
Publication Date: 2009-02-24

Variant appearance in text: rs4657154
PubMed Link: 19204306
Variant Present in the following documents:
  • Main text
View BVdb publication page