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: rs2338971
rs2338971
1.000 0.040 1 101414449 intergenic variant T/A;C snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.810 1.000 1 2014 2016
dbSNP: rs17115100
rs17115100
1.000 0.040 10 102831636 3 prime UTR variant G/T snv 0.14 0.10
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.800 1.000 1 2009 2009
dbSNP: rs4409766
rs4409766
1.000 0.040 10 102856906 intron variant T/C snv 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 1 2009 2009
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: rs12411886
rs12411886
0.882 0.080 10 102925542 intron variant C/A snv 7.8E-02
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 1 2009 2009
dbSNP: rs12413409
rs12413409
0.790 0.200 10 102959339 intron variant G/A snv 9.0E-02
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 1 2009 2009
dbSNP: rs4964469
rs4964469
1.000 0.040 12 106556209 intron variant G/A snv 0.46
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.810 1.000 1 2011 2011
dbSNP: rs1296028
rs1296028
1.000 0.040 8 11841238 downstream gene variant A/G snv 0.20
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.800 1.000 1 2012 2012
dbSNP: rs4837628
rs4837628
1.000 0.040 9 119297431 intron variant T/C snv 0.48
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.800 1.000 1 2010 2010
dbSNP: rs12817488
rs12817488
1.000 0.040 12 122811747 intron variant G/A snv 0.39
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.850 0.857 2 2011 2016
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: rs6430538
rs6430538
0.925 0.080 2 134782397 intron variant C/T snv 0.62
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.830 1.000 1 2012 2019
dbSNP: rs6710823
rs6710823
1.000 0.040 2 134834811 intron variant G/A snv 0.23
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.800 1.000 2 2011 2012
dbSNP: rs1468375
rs1468375
1.000 0.040 7 145337519 intergenic variant C/A;T snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 1 2006 2006
dbSNP: rs2275336
rs2275336
1.000 0.040 6 154405854 3 prime UTR variant G/A snv 6.3E-02
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.800 1.000 1 2012 2012
dbSNP: rs1630500
rs1630500
1.000 0.040 1 154882579 intergenic variant G/A snv 5.0E-02
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.800 1.000 1 2014 2014
dbSNP: rs12726330
rs12726330
1.000 0.040 1 155135691 splice region variant G/A;C snv 1.1E-02; 3.4E-05
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.800 1.000 1 2012 2012
dbSNP: rs7077361
rs7077361
1.000 0.040 10 15519544 intron variant T/C snv 0.11
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 1 2012 2012
dbSNP: rs2823357
rs2823357
1.000 0.040 21 15542586 intron variant G/A snv 0.48
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.810 0.500 1 2011 2019
dbSNP: rs2179030
rs2179030
1.000 0.040 21 15543792 intron variant C/T snv 0.49
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 1 2011 2011
dbSNP: rs34372695
rs34372695
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: 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: rs3213710
rs3213710
1.000 0.040 4 15715698 intron variant G/A snv 0.52 0.44
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 1 2012 2012
dbSNP: rs11931532
rs11931532
1.000 0.040 4 15724143 intron variant T/C snv 0.13
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.730 0.500 1 2012 2019
dbSNP: rs12645693
rs12645693
1.000 0.040 4 15727911 intron variant G/A snv 8.1E-02
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.710 0.500 1 2012 2012