rs920832709, GSN

N. diseases: 4
Disease: Primary Systemic Amyloidosis ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Primary Systemic Amyloidosis
CUI: C0281479
Disease: Primary Systemic Amyloidosis
0.010 GeneticVariation BEFREE Familial amyloidosis of the Finnish type (FAF) is an autosomal dominant type of systemic amyloidosis caused by a G654A (Asn-187) or G654T (Tyr-187) mutation in the gelsolin gene. 9354764 1997