FGB, fibrinogen beta chain, 2244

N. diseases: 95; N. variants: 30
Disease: Dysfibrinogenemia, Congenital ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121909620
rs121909620
Entrez Id: 2244
Gene Symbol: FGB
FGB
CUI: C0272350
Disease:
Dysfibrinogenemia, Congenital 		0.700 GeneticVariation UNIPROT Molecular basis of fibrinogen Naples associated with defective thrombin binding and thrombophilia. Homozygous substitution of B beta 68 Ala----Thr. 1634610 1992