SNCA, synuclein alpha, 6622

N. diseases: 449; N. variants: 66
Disease: Parkinson Disease ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs8180209
rs8180209
Entrez Id: 6622
Gene Symbol: SNCA
SNCA
CUI: C0030567
Disease:
Parkinson Disease 		0.700 GeneticVariation GWASCAT Genome-wide association study of Parkinson's disease in East Asians. 28011712 2017