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: rs356220
rs356220
SNCA ; LOC105377329
0.925 0.080 4 89720189 intron variant T/A;C snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.850 1.000 7 2010 2016