SNCA, synuclein alpha, 6622

N. diseases: 449; N. variants: 66
Disease: Dementia ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104893875
rs104893875
Entrez Id: 6622
Gene Symbol: SNCA
SNCA
CUI: C0497327
Disease:
Dementia 		0.010 GeneticVariation BEFREE Mutations in the gene for α-syn, including the E46K missense mutation, are sufficient to cause Parkinson disease as well as other synucleinopathies like dementia with LBs. 21846727 2011