Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Inherited systemic amyloidosis
CUI: C1719316
Disease: Inherited systemic amyloidosis
0.010 GeneticVariation BEFREE A point mutation (G654A) in the gelsolin gene causes a dominantly inherited systemic amyloidosis called familial amyloidosis of the Finnish type (FAF). 10463954 1999