FGA, fibrinogen alpha chain, 2243

N. diseases: 118; N. variants: 20
Disease: Thrombophilia ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1276352833
rs1276352833
Entrez Id: 2243
Gene Symbol: FGA
FGA
CUI: C0398623
Disease:
Thrombophilia 		0.010 GeneticVariation BEFREE Exome Sequencing and Clot Lysis Experiments Demonstrate the R458C Mutation of the Alpha Chain of Fibrinogen to be Associated with Impaired Fibrinolysis in a Family with Thrombophilia. 26581183 2016