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: 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: 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: 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: rs12364577
rs12364577
1.000 0.040 11 49685809 intron variant A/C snv 0.35
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 1 2006 2006
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: 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: rs2666781
rs2666781
1.000 0.040 10 21916747 intron variant C/A snv 0.58
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 1 2006 2006
dbSNP: rs2862909
rs2862909
1.000 0.040 13 24527029 intron variant G/T snv 0.63
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 1 2006 2006
dbSNP: rs4746675
rs4746675
1.000 0.040 10 67192300 intron variant C/A snv 0.37
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 1 2006 2006
dbSNP: rs557074
rs557074
1.000 0.040 6 7144958 intron variant T/G snv 0.27
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 1 2006 2006
dbSNP: rs6460033
rs6460033
1.000 0.040 7 72798898 intron variant A/C snv 0.69
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 1 2006 2006
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: rs7846412
rs7846412
1.000 0.040 8 91032300 intron variant A/G snv 0.47
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 1 2006 2006
dbSNP: rs850084
rs850084
1.000 0.040 7 29731981 non coding transcript exon variant A/C snv 0.27
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 1 2006 2006
dbSNP: rs9952724
rs9952724
1.000 0.040 18 48726444 intron variant A/C;T 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: 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: 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: 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: 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: rs870575
rs870575
1.000 0.040 2 45276121 intron variant G/A;C snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 1 2010 2010