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: rs10014396
rs10014396
Entrez Id: 6622
Gene Symbol: SNCA
SNCA
CUI: C0030567
Disease:
Parkinson Disease 		0.010 GeneticVariation BEFREE A number of SNCA variants, not including rs10014396 or rs3775439, were significantly associated with susceptibility to PD. 22912757 2012