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: rs356168
rs356168
SNCA
1.000 0.040 4 89753280 intron variant G/A snv 0.45
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.710 1.000 2 2010 2017