FGB, fibrinogen beta chain, 2244

N. diseases: 95; N. variants: 30
Disease: Congenital hypofibrinogenemia ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs6054
rs6054
Entrez Id: 2244
Gene Symbol: FGB
FGB
CUI: C2584774
Disease:
Congenital hypofibrinogenemia 		T 0.700 CausalMutation CLINVAR