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: rs894278
rs894278
SNCA
0.882 0.080 4 89813384 intron variant T/G snv 0.15
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.720 1.000 3 2009 2019