KAT2B c.430+7398C>T

Variant ID: 3-20121349-C-T

NM_003884.4(KAT2B):c.430+7398C>T

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Genetic risk factors for restenosis after percutaneous coronary intervention in Kazakh population.

Human Genomics
Zholdybayeva, Elena V EV; Talzhanov, Yerkebulan A YA; Aitkulova, Akbota M AM; Tarlykov, Pavel V PV; Kulmambetova, Gulmira N GN; Iskakova, Aisha N AN; Dzholdasbekova, Aliya U AU; Visternichan, Olga A OA; Taizhanova, Dana Zh DZh; Ramanculov, Yerlan M YM
Publication Date: 2016-06-08

Variant appearance in text: rs17796904
PubMed Link: 27277665
Variant Present in the following documents:
  • Main text
  • 40246_2016_Article_77.pdf
View BVdb publication page



Genetics of coronary artery disease and myocardial infarction.

World Journal Of Cardiology
Dai, Xuming X; Wiernek, Szymon S; Evans, James P JP; Runge, Marschall S MS
Publication Date: 2016-01-26

Variant appearance in text: rs17796904
PubMed Link: 26839654
Variant Present in the following documents:
  • Main text
View BVdb publication page



Systematic testing of literature reported genetic variation associated with coronary restenosis: results of the GENDER Study.

Plos One
Verschuren, Jeffrey J W JJ; Trompet, Stella S; Postmus, Iris I; Sampietro, M Lourdes ML; Heijmans, Bastiaan T BT; Houwing-Duistermaat, Jeanine J JJ; Slagboom, P Eline PE; Jukema, J Wouter JW
Publication Date: 2012

Variant appearance in text: rs17796904
PubMed Link: 22879966
Variant Present in the following documents:
  • Main text
  • pone.0042401.pdf
View BVdb publication page