NOS1AP c.177+30953C>T

Variant ID: 1-162155219-C-T

NM_014697.2(NOS1AP):c.177+30953C>T

This variant was identified in 2 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: rs7412698
PubMed Link: 23347024
Variant Present in the following documents:
  • Main text
View BVdb publication page



Common variants in CASQ2, GPD1L, and NOS1AP are significantly associated with risk of sudden death in patients with coronary artery disease.

Circulation. Cardiovascular Genetics
Westaway, Shawn K SK; Reinier, Kyndaron K; Huertas-Vazquez, Adriana A; Evanado, Audrey A; Teodorescu, Carmen C; Navarro, Jo J; Sinner, Moritz F MF; Gunson, Karen K; Jui, Jonathan J; Spooner, Peter P; Kaab, Stefan S; Chugh, Sumeet S SS
Publication Date: 2011-08-01

Variant appearance in text: rs7412698
PubMed Link: 21685173
Variant Present in the following documents:
  • Main text
View BVdb publication page