Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104893877
rs104893877
0.030 GeneticVariation BEFREE Mice overexpressing the human A53T mutant alpha-Syn develop a severe movement disorder, paralysis, and synucleinopathy, but the mechanisms are not understood. 16399671

2006

dbSNP: rs104893877
rs104893877
0.030 GeneticVariation BEFREE Mice carrying an Ala53Thr human SNCA transgene driven by the mouse prion promoter show a mild movement disorder and only rarely develop severe pathology by 2 years of age. 15585343

2005

dbSNP: rs104893877
rs104893877
0.030 GeneticVariation BEFREE Neuronal alpha-synucleinopathy with severe movement disorder in mice expressing A53T human alpha-synuclein. 12062037

2002