EPHB4 c.2119-942T>C

Variant ID: 7-100406144-A-G

NM_004444.4(EPHB4):c.2119-942T>C

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Methodological quality assessment of genetic studies on brain arteriovenous malformation related hemorrhage: A cross-sectional study.

Frontiers In Genetics
Jiang, Junhao J; Qin, Zhuo Z; Yan, Junxia J; Liu, Junyu J
Publication Date: 2023

Variant appearance in text: rs314353
PubMed Link: 37065486
Variant Present in the following documents:
  • Main text
  • fgene-14-1123898.pdf
View BVdb publication page



EPHB4 gene polymorphisms and risk of intracranial hemorrhage in patients with brain arteriovenous malformations.

Circulation. Cardiovascular Genetics
Weinsheimer, Shantel S; Kim, Helen H; Pawlikowska, Ludmila L; Chen, Yongmei Y; Lawton, Michael T MT; Sidney, Stephen S; Kwok, Pui-Yan PY; McCulloch, Charles E CE; Young, William L WL
Publication Date: 2009-10

Variant appearance in text: rs314353
PubMed Link: 20031623
Variant Present in the following documents:
  • Main text
View BVdb publication page