VWF c.7438-1924T>C

Variant ID: 12-6082799-A-G

NM_000552.3(VWF):c.7438-1924T>C

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Noninvasive fetal genotyping of single nucleotide variants and linkage analysis for prenatal diagnosis of monogenic disorders.

Human Genomics
Wu, Wenman W; Zhou, Xuanyou X; Jiang, Zhengwen Z; Zhang, Dazhi D; Yu, Feng F; Zhang, Lanlan L; Wang, Xuefeng X; Chen, Songchang S; Xu, Chenming C
Publication Date: 2022-07-27

Variant appearance in text: rs12829271
PubMed Link: 35897115
Variant Present in the following documents:
  • 40246_2022_Article_400.pdf
  • 40246_2022_400_MOESM5_ESM.xlsx, sheet 1
  • 40246_2022_400_MOESM1_ESM.xlsx, sheet 1
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: rs12829271
PubMed Link: 27224245
Variant Present in the following documents:
  • Main text
  • pone.0155832.pdf
View BVdb publication page