F8 c.2113+2443C>T

Variant ID: X-154173530-G-A

NM_000132.3(F8):c.2113+2443C>T

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Violating the theory of single gene-single disorder: inhibitor development in hemophilia.

Indian Journal Of Hematology & Blood Transfusion : An Official Journal Of Indian Society Of Hematology And Blood Transfusion
AlFadhli, Suad S; Nizam, Rasheeba R
Publication Date: 2015-06

Variant appearance in text: rs6643622
PubMed Link: 25825553
Variant Present in the following documents:
  • Main text
View BVdb publication page



Influence of single nucleotide polymorphisms in factor VIII and von Willebrand factor genes on plasma factor VIII activity: the ARIC Study.

Blood
Campos, Marco M; Buchanan, Ashley A; Yu, Fuli F; Barbalic, Maja M; Xiao, Yang Y; Chambless, Lloyd E LE; Wu, Kenneth K KK; Folsom, Aaron R AR; Boerwinkle, Eric E; Dong, Jing-fei JF
Publication Date: 2012-02-23

Variant appearance in text: rs6643622
PubMed Link: 22219226
Variant Present in the following documents:
  • Main text
View BVdb publication page



A case-control study reveals immunoregulatory gene haplotypes that influence inhibitor risk in severe haemophilia A.

Haemophilia : The Official Journal Of The World Federation Of Hemophilia
Lozier, J N JN; Rosenberg, P S PS; Goedert, J J JJ; Menashe, I I
Publication Date: 2011-07

Variant appearance in text: rs6643622
PubMed Link: 21362111
Variant Present in the following documents:
  • Main text
View BVdb publication page