NOS1AP c.105+6063C>G

Variant ID: 1-162046135-C-G

NM_014697.2(NOS1AP):c.105+6063C>G

This variant was identified in 6 publications

View GRCh38 version.




Publications:


KCNQ1 and Long QT Syndrome in 1/45 Amish: The Road From Identification to Implementation of Culturally Appropriate Precision Medicine.

Circulation. Genomic And Precision Medicine
Streeten, Elizabeth A EA; See, Vincent Y VY; Jeng, Linda B J LBJ; Maloney, Kristin A KA; Lynch, Megan M; Glazer, Andrew M AM; Yang, Tao T; Roden, Dan D; Pollin, Toni I TI; Daue, Melanie M; Ryan, Kathleen A KA; Van Hout, Cristopher C; Gosalia, Nehal N; Gonzaga-Jauregui, Claudia C; Economides, Aris A; Perry, James A JA; O'Connell, Jeffrey J; Beitelshees, Amber A; Palmer, Kathleen K; Mitchell, Braxton D BD; Shuldiner, Alan R AR; ,
Publication Date: 2020-12

Variant appearance in text: rs1415262
PubMed Link: 33141630
Variant Present in the following documents:
  • hcg-13-e003133-s001.pdf
View BVdb publication page



Nitric Oxide Synthase 1 Adaptor Protein, an Emerging New Genetic Marker for QT Prolongation and Sudden Cardiac Death.

Acta Cardiologica Sinica
Chang, Kuan-Cheng KC; Sasano, Tetsuo T; Wang, Yu-Chen YC; Huang, Shoei K Stephen SK
Publication Date: 2013-05

Variant appearance in text: rs1415262
PubMed Link: 27122710
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: rs1415262
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: rs1415262
PubMed Link: 19204306
Variant Present in the following documents:
  • Main text
View BVdb publication page



Multiple independent genetic factors at NOS1AP modulate the QT interval in a multi-ethnic population.

Plos One
Arking, Dan E DE; Khera, Amit A; Xing, Chao C; Kao, W H Linda WH; Post, Wendy W; Boerwinkle, Eric E; Chakravarti, Aravinda A
Publication Date: 2009

Variant appearance in text: rs1415262
PubMed Link: 19180230
Variant Present in the following documents:
  • Main text
  • pone.0004333.pdf
View BVdb publication page



Associations between genetic variants in the NOS1AP (CAPON) gene and cardiac repolarization in the old order Amish.

Human Heredity
Post, Wendy W; Shen, Haiqing H; Damcott, Coleen C; Arking, Dan E DE; Kao, W H Linda WH; Sack, Paul A PA; Ryan, Kathleen A KA; Chakravarti, Aravinda A; Mitchell, Braxton D BD; Shuldiner, Alan R AR
Publication Date: 2007

Variant appearance in text: rs1415262
PubMed Link: 17565224
Variant Present in the following documents:
  • Main text
View BVdb publication page