VWF c.1533+2387A>G

Variant ID: 12-6169733-T-C

NM_000552.3(VWF):c.1533+2387A>G

This variant was identified in 4 publications

View GRCh38 version.




Publications:


Coagulation factor VIII: Relationship to cardiovascular disease risk and whole genome sequence and epigenome-wide analysis in African Americans.

Journal Of Thrombosis And Haemostasis : Jth
Raffield, Laura M LM; Lu, Ake T AT; Szeto, Mindy D MD; Little, Amarise A; Grinde, Kelsey E KE; Shaw, Jessica J; Auer, Paul L PL; Cushman, Mary M; Horvath, Steve S; Irvin, Marguerite R MR; Lange, Ethan M EM; Lange, Leslie A LA; Nickerson, Deborah A DA; Thornton, Timothy A TA; Wilson, James G JG; Wheeler, Marsha M MM; , ; Zakai, Neil A NA; Reiner, Alex P AP
Publication Date: 2020-06

Variant appearance in text: rs4764482
PubMed Link: 31985870
Variant Present in the following documents:
  • Main text
View BVdb publication page



Von Willebrand Factor Gene Variants Associate with Herpes simplex Encephalitis.

Plos One
Abdelmagid, Nada N; Bereczky-Veress, Biborka B; Atanur, Santosh S; Musilová, Alena A; Zídek, Václav V; Saba, Laura L; Warnecke, Andreas A; Khademi, Mohsen M; Studahl, Marie M; Aurelius, Elisabeth E; Hjalmarsson, Anders A; Garcia-Diaz, Ana A; Denis, Cécile V CV; Bergström, Tomas T; Sköldenberg, Birgit B; Kockum, Ingrid I; Aitman, Timothy T; Hübner, Norbert N; Olsson, Tomas T; Pravenec, Michal M; Diez, Margarita M
Publication Date: 2016

Variant appearance in text: rs4764482
PubMed Link: 27224245
Variant Present in the following documents:
  • Main text
  • pone.0155832.pdf
View BVdb publication page



Gene-centric approach identifies new and known loci for FVIII activity and VWF antigen levels in European Americans and African Americans.

American Journal Of Hematology
Tang, Weihong W; Cushman, Mary M; Green, David D; Rich, Stephen S SS; Lange, Leslie A LA; Yang, Qiong Q; Tracy, Russell P RP; Tofler, Geoffrey H GH; Basu, Saonli S; Wilson, James G JG; Keating, Brendan J BJ; Weng, Lu-Chen LC; Taylor, Herman A HA; Jacobs, David R DR; Delaney, Joseph A JA; Palmer, Cameron D CD; Young, Taylor T; Pankow, James S JS; O'Donnell, Christopher J CJ; Smith, Nicholas L NL; Reiner, Alexander P AP; Folsom, Aaron R AR
Publication Date: 2015-06

Variant appearance in text: rs4764482
PubMed Link: 25779970
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic associations with expression for genes implicated in GWAS studies for atherosclerotic cardiovascular disease and blood phenotypes.

Human Molecular Genetics
Zhang, Xiaoling X; Johnson, Andrew D AD; Hendricks, Audrey E AE; Hwang, Shih-Jen SJ; Tanriverdi, Kahraman K; Ganesh, Santhi K SK; Smith, Nicholas L NL; Peyser, Patricia A PA; Freedman, Jane E JE; O'Donnell, Christopher J CJ
Publication Date: 2014-02-01

Variant appearance in text: rs4764482
PubMed Link: 24057673
Variant Present in the following documents:
  • Main text
View BVdb publication page