rs121909715, GSN

N. diseases: 8
Disease: Meretoja syndrome ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Meretoja syndrome
CUI: C1622345
Disease: Meretoja syndrome
0.800 GeneticVariation UNIPROT Gelsolin-derived familial amyloidosis caused by asparagine or tyrosine substitution for aspartic acid at residue 187. 1338910 1992
Meretoja syndrome
CUI: C1622345
Disease: Meretoja syndrome
0.800 GeneticVariation UNIPROT Gelsolin variant (Asn-187) in familial amyloidosis, Finnish type. 2176481 1990
Meretoja syndrome
CUI: C1622345
Disease: Meretoja syndrome
0.800 CausalMutation CLINVAR
Meretoja syndrome
CUI: C1622345
Disease: Meretoja syndrome
0.800 CausalMutation CLINVAR