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: rs356174
rs356174
SNCA ; LOC105377329
1.000 0.040 4 89709750 intron variant G/T snv 0.72
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 1.000 1 2011 2011
dbSNP: rs356169
rs356169
SNCA ; LOC105377329
1.000 0.040 4 89711617 intron variant G/T snv 0.72
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 1.000 1 2011 2011
dbSNP: rs2572323
rs2572323
SNCA ; LOC105377329
1.000 0.040 4 89713401 intron variant A/G snv 0.75
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 1.000 1 2011 2011
dbSNP: rs1372519
rs1372519
SNCA ; SNCA-AS1
1.000 0.040 4 89836158 5 prime UTR variant A/G snv 0.77
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 1.000 1 2011 2011
dbSNP: rs356180
rs356180
SNCA ; LOC105377329
1.000 0.040 4 89706976 intron variant A/G snv 0.77
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 1.000 1 2011 2011
dbSNP: rs1372520
rs1372520
SNCA ; SNCA-AS1
1.000 0.040 4 89836354 intron variant T/C snv 0.78
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 1.000 1 2011 2011
dbSNP: rs2197120
rs2197120
SNCA
1.000 0.040 4 89808451 intron variant A/G snv 0.78
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 1.000 2 2011 2012
dbSNP: rs168552
rs168552
SNCA ; LOC105377329
1.000 0.040 4 89721993 intron variant C/T snv 0.80
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 1.000 1 2011 2011