VWF c.2187-652T>C

Variant ID: 12-6156635-A-G

NM_000552.3(VWF):c.2187-652T>C

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Genetic determinants of plasma von Willebrand factor antigen levels: a target gene SNP and haplotype analysis of ARIC cohort.

Blood
Campos, Marco M; Sun, Wei W; Yu, Fuli F; Barbalic, Maja M; Tang, Weihong W; Chambless, Lloyd E LE; Wu, Kenneth K KK; Ballantyne, Christie C; Folsom, Aaron R AR; Boerwinkle, Eric E; Dong, Jing-Fei JF
Publication Date: 2011-05-12

Variant appearance in text: rs216299
PubMed Link: 21343614
Variant Present in the following documents:
  • Main text
View BVdb publication page



A common variant in the Von Willebrand factor gene is associated with multiple functional consequences.

American Journal Of Hematology
Vaidya, Dhananjay D; Yanek, Lisa R LR; Herrera-Galeano, J Enrique JE; Mathias, Rasika A RA; Moy, Taryn F TF; Faraday, Nauder N; Becker, Lewis C LC; Becker, Diane M DM
Publication Date: 2010-12

Variant appearance in text: rs216299
PubMed Link: 20941784
Variant Present in the following documents:
  • Main text
View BVdb publication page