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: rs393152
rs393152
LINC02210 ; LINC02210-CRHR1
0.851 0.160 17 45641777 non coding transcript exon variant A/G snv 0.18 0.29
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.810 1.000 3 2009 2015
dbSNP: rs546433642
rs546433642
KANSL1
0.925 0.120 17 46172742 intron variant T/C;G snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 1.000 3 2009 2012
dbSNP: rs549599956
rs549599956
KANSL1
0.925 0.120 17 46169798 intron variant A/G snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 1.000 3 2009 2012
dbSNP: rs7224296
rs7224296
NSF ; LRRC37A2
0.882 0.160 17 46722680 intron variant G/A snv 0.59
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 1.000 3 2009 2012
dbSNP: rs7225002
rs7225002
KANSL1
0.925 0.080 17 46111701 intron variant A/G snv 0.39
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 1.000 3 2009 2012
dbSNP: rs894278
rs894278
SNCA
0.882 0.080 4 89813384 intron variant T/G snv 0.15
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.720 1.000 3 2009 2019
dbSNP: rs11240572
rs11240572
PM20D1 ; LOC107985250
1.000 0.040 1 205838885 intron variant C/A;T snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.730 1.000 2 2009 2016
dbSNP: rs11248060
rs11248060
DGKQ
1.000 0.040 4 970571 intron variant C/T snv 9.3E-02
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.810 1.000 2 2012 2013
dbSNP: rs12644119
rs12644119
LOC105377329
1.000 0.040 4 89682268 intron variant C/A snv 0.17
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 1.000 2 2009 2012
dbSNP: rs1526123
rs1526123
LINC02210-CRHR1
1.000 0.040 17 45705974 intron variant T/C snv 0.55
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 1.000 2 2009 2012
dbSNP: rs16940665
rs16940665
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
1.000 0.040 17 45830530 stop lost T/C snv 0.15 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 1.000 2 2011 2012
dbSNP: rs1800547
rs1800547
MAPT
0.925 0.120 17 45974480 non coding transcript exon variant A/G snv 0.15 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.720 1.000 2 2008 2012
dbSNP: rs181489
rs181489
SNCA ; LOC105377329
1.000 0.040 4 89713869 intron variant T/A;C snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.710 1.000 2 2011 2015
dbSNP: rs1876828
rs1876828
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
0.851 0.160 17 45834159 intron variant C/T snv 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 1.000 2 2011 2012
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: rs2708453
rs2708453
SLC2A13 ; LOC112268095
1.000 0.040 12 40084850 intron variant G/T snv 0.12
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 1.000 2 2012 2014
dbSNP: rs2737029
rs2737029
SNCA
1.000 0.040 4 89790619 intron variant T/C snv 0.45
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.720 1.000 2 2008 2018
dbSNP: rs34372695
rs34372695
RAB25
1.000 0.040 1 156060246 upstream gene variant C/G;T snv 1.5E-02
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.810 1.000 2 2011 2012
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
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
dbSNP: rs356221
rs356221
SNCA ; LOC105377329
1.000 0.040 4 89721313 intron variant A/T snv 0.44
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.710 1.000 2 2011 2013
dbSNP: rs3822086
rs3822086
SNCA
1.000 0.040 4 89743643 intron variant C/T snv 0.24
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.730 1.000 2 2011 2019
dbSNP: rs415430
rs415430
WNT3 ; LRRC37A2
1.000 0.040 17 46781778 intron variant C/T snv 0.84
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.800 1.000 2 2011 2011
dbSNP: rs4525537
rs4525537
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
1.000 0.040 17 45835357 3 prime UTR variant T/C snv 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 1.000 2 2011 2012
dbSNP: rs4538475
rs4538475
BST1
1.000 0.040 4 15736314 intron variant A/G snv 0.24
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.810 1.000 2 2009 2012