FGB, fibrinogen beta chain, 2244

N. diseases: 95; N. variants: 30
Disease: Fibrinogen, CTCAE ×
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: C1561955
Disease:
Fibrinogen, CTCAE 		0.700 GeneticVariation GWASDB We identified a rare Pro265Leu variant in FGB (rs6054) associated with lower fibrinogen. 20978265 2011