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: rs417968
rs417968
1.000 0.040 17 45651010 non coding transcript exon variant G/A snv 0.65
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 5 2009 2014
dbSNP: rs17563986
rs17563986
1.000 0.040 17 45913906 intron variant A/G snv 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 4 2009 2014
dbSNP: rs7215239
rs7215239
1.000 0.040 17 45690407 intron variant T/C snv 0.30
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 4 2011 2014
dbSNP: rs12373139
rs12373139
0.925 0.120 17 45846764 missense variant G/A snv 0.15 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 3 2009 2012
dbSNP: rs169201
rs169201
0.925 0.160 17 46712837 intron variant A/G snv 0.13
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 3 2009 2012
dbSNP: rs17690703
rs17690703
0.882 0.160 17 45847931 intron variant C/T snv 0.18
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 3 2009 2012
dbSNP: rs1981997
rs1981997
1.000 0.040 17 45979401 non coding transcript exon variant G/A snv 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 3 2009 2012
dbSNP: rs2668692
rs2668692
1.000 0.040 17 46215654 intron variant G/A;T snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 3 2009 2012
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: rs546433642
rs546433642
0.925 0.120 17 46172742 intron variant T/C;G snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 3 2009 2012
dbSNP: rs549599956
rs549599956
0.925 0.120 17 46169798 intron variant A/G snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 3 2009 2012
dbSNP: rs7224296
rs7224296
0.882 0.160 17 46722680 intron variant G/A snv 0.59
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 3 2009 2012
dbSNP: rs7225002
rs7225002
0.925 0.080 17 46111701 intron variant A/G snv 0.39
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 3 2009 2012
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: rs1526123
rs1526123
1.000 0.040 17 45705974 intron variant T/C snv 0.55
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 2 2009 2012
dbSNP: rs16940665
rs16940665
1.000 0.040 17 45830530 stop lost T/C snv 0.15 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 2 2011 2012
dbSNP: rs1876828
rs1876828
0.851 0.160 17 45834159 intron variant C/T snv 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 2 2011 2012
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: rs2708453
rs2708453
1.000 0.040 12 40084850 intron variant G/T snv 0.12
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 2 2012 2014
dbSNP: rs4525537
rs4525537
1.000 0.040 17 45835357 3 prime UTR variant T/C snv 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 2 2011 2012
dbSNP: rs4768212
rs4768212
1.000 0.040 12 40080345 intron variant C/T snv 0.95
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 2 2012 2014
dbSNP: rs878887
rs878887
1.000 0.040 17 45835216 3 prime UTR variant C/T snv 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 2 2011 2012
dbSNP: rs878888
rs878888
1.000 0.040 17 45835269 3 prime UTR variant A/G snv 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 2 2011 2012
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