Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs950592627
rs950592627
APP
CUI: C0740340
Disease: Amyloidosis, Familial
Amyloidosis, Familial 		0.010 GeneticVariation BEFREE Furthermore, a second peptide with a substitution similar to that in the Dutch-type hereditary amyloidosis mutation (Glu22 to Gln) was also found to be a substrate for transglutaminase. 7922559

1994