FGA, fibrinogen alpha chain, 2243

N. diseases: 118; N. variants: 20
Disease: Systemic amyloidosis ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121909612
rs121909612
Entrez Id: 2243
Gene Symbol: FGA
FGA
CUI: C0268380
Disease:
Systemic amyloidosis 		0.010 GeneticVariation BEFREE Curative hepatorenal transplantation in systemic amyloidosis caused by the Glu526Val fibrinogen alpha-chain variant in an English family. 10825402 2000