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: rs2736990
rs2736990
SNCA
0.882 0.080 4 89757390 intron variant G/A;T snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.860 1.000 6 2009 2018
dbSNP: rs2736990
rs2736990
SNCA
0.882 0.080 4 89757390 intron variant G/A;T snv
CUI: C0162534
Disease: Prion Diseases
Prion Diseases 		0.700 1.000 1 2012 2012