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: rs7684318
rs7684318
SNCA
1.000 0.040 4 89733852 intron variant T/C snv 0.19
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.730 1.000 1 2006 2012