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: rs356203
rs356203
SNCA
1.000 0.040 4 89744890 intron variant C/T snv 0.54
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.800 1.000 2 2011 2019