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: rs6532197
rs6532197
1.000 0.040 4 89876150 upstream gene variant A/G snv 0.16
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.800 1.000 2 2009 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: 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: rs12063142
rs12063142
1.000 0.040 1 18813023 intergenic variant C/T snv 0.28
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.800 1.000 1 2010 2010
dbSNP: rs12069733
rs12069733
1.000 0.040 1 43475837 TF binding site variant G/A snv 0.37
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 1 2006 2006
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: rs13227860
rs13227860
1.000 0.040 7 22114836 downstream gene variant G/A snv 0.26
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 1 2006 2006
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: rs1504212
rs1504212
1.000 0.040 5 53824125 upstream gene variant C/A snv 0.51
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 1 2006 2006
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: rs213462
rs213462
1.000 0.040 X 83449447 intergenic variant A/C snv 0.50
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 1 2006 2006
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: rs2395163
rs2395163
0.882 0.160 6 32420032 intergenic variant T/C snv 0.17
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.820 1.000 1 2012 2020
dbSNP: rs6532194
rs6532194
1.000 0.040 4 89859751 intergenic variant C/G;T snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.800 1.000 1 2012 2012
dbSNP: rs6757197
rs6757197
1.000 0.040 2 158866994 intron variant G/C;T snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 1 2006 2006
dbSNP: rs823122
rs823122
1.000 0.040 1 205755900 intergenic variant C/T snv 0.83
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.710 1.000 1 2011 2012
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: 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: 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: 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: 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: 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: rs4538475
rs4538475
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
dbSNP: rs4698412
rs4698412
1.000 0.040 4 15735725 intron variant G/A;T snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.850 1.000 2 2011 2019
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