FGG, fibrinogen gamma chain, 2266

N. diseases: 70; N. variants: 18
Disease: Hypodysfibrinogenemia ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587777720
rs587777720
Entrez Id: 2266
Gene Symbol: FGG
FGG
CUI: C0472803
Disease:
Hypodysfibrinogenemia 		G 0.700 CausalMutation CLINVAR