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: rs3772715
rs3772715
1.000 0.040 3 183131776 intron variant C/T snv 0.76
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 1 2011 2011
dbSNP: rs482912
rs482912
1.000 0.040 3 183135882 missense variant T/C snv 0.65 0.59
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 1 2011 2011
dbSNP: rs7640612
rs7640612
1.000 0.040 3 183025479 intron variant C/A snv 0.50
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 1 2011 2011
dbSNP: rs9822789
rs9822789
1.000 0.040 3 183085086 intron variant G/T snv 0.17
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 1 2011 2011
dbSNP: rs9841498
rs9841498
1.000 0.040 3 183009309 intergenic variant C/T snv 0.43
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 1 2011 2011
dbSNP: rs9878775
rs9878775
1.000 0.040 3 182942165 3 prime UTR variant T/A;C snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 1 2011 2011
dbSNP: rs356220
rs356220
0.925 0.080 4 89720189 intron variant T/A;C snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.850 1.000 7 2010 2016
dbSNP: rs2736990
rs2736990
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: rs11931074
rs11931074
0.851 0.080 4 89718364 intron variant G/A;C;T snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.900 1.000 4 2009 2020
dbSNP: rs356219
rs356219
0.776 0.240 4 89716450 intron variant G/A snv 0.54
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.900 1.000 4 2008 2019
dbSNP: rs11724635
rs11724635
0.925 0.080 4 15735478 intron variant C/A;G snv 0.43
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.880 0.846 3 2011 2019
dbSNP: rs356229
rs356229
1.000 0.040 4 89685446 non coding transcript exon variant C/A;T snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 3 2009 2012
dbSNP: rs3775439
rs3775439
1.000 0.040 4 89788590 intron variant G/A snv 0.25
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.710 1.000 3 2009 2012
dbSNP: rs3857059
rs3857059
1.000 0.040 4 89754087 intron variant A/G;T snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.710 1.000 3 2009 2016
dbSNP: rs894278
rs894278
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: rs11248060
rs11248060
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
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: rs1564282
rs1564282
GAK
1.000 0.040 4 858525 intron variant C/T snv 8.1E-02
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.870 0.889 2 2009 2015
dbSNP: rs181489
rs181489
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: rs2197120
rs2197120
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: rs2737029
rs2737029
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: rs356165
rs356165
0.882 0.080 4 89725735 3 prime UTR variant G/A snv 0.54
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.780 0.900 2 2007 2015
dbSNP: rs356168
rs356168
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
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
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