Source: UNIPROT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121909612
rs121909612
FGA
CUI: C0268389
Disease: Amyloidosis, familial visceral
Amyloidosis, familial visceral 		0.800 GeneticVariation UNIPROT Hereditary renal amyloidosis associated with a mutant fibrinogen alpha-chain. 8097946

1993