rs1418203843, SNCA

N. diseases: 1
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Parkinson Disease, Familial, Type 1
CUI: C3489791
Disease: Parkinson Disease, Familial, Type 1
0.010 GeneticVariation BEFREE We found one change (G199A) in exon 4 in one family with a pattern of autosomal dominant PD. 11748744 2001