rs920832709, GSN

N. diseases: 4
Disease: Systemic amyloidosis ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Systemic amyloidosis
CUI: C0268380
Disease: 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