ATP1B1 c.227-565T>A

Variant ID: 1-169093557-T-A

NM_001677.3(ATP1B1):c.227-565T>A

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Prioritization of causal genes for coronary artery disease based on cumulative evidence from experimental and in silico studies.

Scientific Reports
Shadrina, Alexandra S AS; Shashkova, Tatiana I TI; Torgasheva, Anna A AA; Sharapov, Sodbo Z SZ; Klarić, Lucija L; Pakhomov, Eugene D ED; Alexeev, Dmitry G DG; Wilson, James F JF; Tsepilov, Yakov A YA; Joshi, Peter K PK; Aulchenko, Yurii S YS
Publication Date: 2020-06-26

Variant appearance in text: rs10919065
PubMed Link: 32591598
Variant Present in the following documents:
  • Main text
  • 41598_2020_67001_MOESM6_ESM.pdf
View BVdb publication page



Single nucleotide polymorphism-single nucleotide polymorphism interactions among inflammation genes in the genetic architecture of blood pressure in the Framingham Heart Study.

American Journal Of Hypertension
Basson, Jacob J JJ; de Las Fuentes, Lisa L; Rao, Dabeeru C DC
Publication Date: 2015-02

Variant appearance in text: rs10919065
PubMed Link: 25063733
Variant Present in the following documents:
  • Main text
View BVdb publication page