rs542171324, SNCA

N. diseases: 6
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Fibrillation
CUI: C0232197
Disease: Fibrillation
0.010 GeneticVariation BEFREE Our data suggest that the A53V mutation accelerates fibrillation of α-Syn without affecting the overall morphology or cytotoxicity of fibrils compared to those of the wild-type (WT) protein. 29771508 2018