FGG, fibrinogen gamma chain, 2266

N. diseases: 70; N. variants: 18
Disease: Congenital hypofibrinogenemia ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs148685782
rs148685782
Entrez Id: 2266
Gene Symbol: FGG
FGG
CUI: C2584774
Disease:
Congenital hypofibrinogenemia 		C 0.700 CausalMutation CLINVAR