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F8 c.143+2402C>T
Variant ID: X-154248283-G-A
NM_000132.3(
F8
):c.143+2402C>T
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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: rs6649625
PubMed Link:
25825553
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: rs6649625
PubMed Link:
21362111
Variant Present in the following documents:
Main text
View BVdb publication page