Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs356221
rs356221
SNCA ; LOC105377329
1.000 0.040 4 89721313 intron variant A/T snv 0.44
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.710 1.000 2 2011 2013