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: rs10445337
rs10445337
0.925 0.120 17 45990034 missense variant T/C snv 0.15 0.15
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 1 2012 2012
dbSNP: rs10445338
rs10445338
1.000 0.040 17 45990316 intron variant G/A snv 0.15
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 1 2012 2012
dbSNP: rs10445364
rs10445364
1.000 0.040 17 45838990 intron variant G/A;C snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 1 2012 2012
dbSNP: rs10506095
rs10506095
1.000 0.040 12 32647193 downstream gene variant C/T snv 4.4E-02
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 1 2014 2014
dbSNP: rs10513789
rs10513789
1.000 0.040 3 183042285 intron variant T/G snv 0.22
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.800 1.000 1 2011 2011
dbSNP: rs10516839
rs10516839
1.000 0.040 4 89587189 intron variant T/G snv 0.17
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 1 2011 2011
dbSNP: rs10516845
rs10516845
1.000 0.040 4 89763127 intron variant A/G;T snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 1 2011 2011
dbSNP: rs10518765
rs10518765
1.000 0.040 15 54388434 intron variant A/C snv 0.16
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 1 2006 2006
dbSNP: rs10519131
rs10519131
1.000 0.040 15 61708933 intron variant A/C;T snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.800 1.000 1 2012 2012
dbSNP: rs1052551
rs1052551
1.000 0.040 17 45991558 synonymous variant G/A;T snv 0.14; 8.0E-05
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 1 2012 2012
dbSNP: rs1052553
rs1052553
0.827 0.200 17 45996523 synonymous variant A/G snv 0.14 0.15
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.730 0.750 1 2010 2012
dbSNP: rs1052587
rs1052587
0.925 0.120 17 46025238 3 prime UTR variant T/C snv 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 1 2012 2012
dbSNP: rs10737170
rs10737170
1.000 0.040 1 156094089 intron variant C/A snv 0.90
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 1 2014 2014
dbSNP: rs1078268
rs1078268
MAPT ; STH
0.925 0.120 17 45998535 intron variant A/G snv 0.15
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 1 2012 2012
dbSNP: rs10847864
rs10847864
1.000 0.040 12 122842051 intron variant G/A;C;T snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 1 2012 2012
dbSNP: rs10877840
rs10877840
1.000 0.040 12 39959194 intron variant T/C snv 0.19
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.800 1.000 1 2012 2012
dbSNP: rs10963676
rs10963676
1.000 0.040 9 18622045 intron variant T/C;G snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 1 2006 2006
dbSNP: rs11012
rs11012
1.000 0.040 17 45436075 3 prime UTR variant C/T snv 0.13 0.13
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.800 1.000 4 2009 2012
dbSNP: rs11191425
rs11191425
1.000 0.040 10 102866213 intron variant C/T snv 1.0E-01
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 1 2009 2009
dbSNP: rs11209290
rs11209290
1.000 0.040 1 68405344 intergenic variant G/A snv 6.7E-02
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 1 2011 2011
dbSNP: rs11240572
rs11240572
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: rs11248051
rs11248051
GAK
1.000 0.040 4 864544 intron variant C/G;T snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.820 1.000 1 2010 2014
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: rs11564273
rs11564273
1.000 0.040 12 40204350 intron variant T/G snv 6.5E-02
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 1 2012 2012
dbSNP: rs11711441
rs11711441
1.000 0.040 3 183103487 intron variant G/A snv 0.12
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.810 1.000 3 2011 2013