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: rs11931074
rs11931074
SNCA ; LOC105377329
0.851 0.080 4 89718364 intron variant G/A;C;T snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.900 1.000 4 2009 2020
dbSNP: rs356219
rs356219
SNCA ; LOC105377329
0.776 0.240 4 89716450 intron variant G/A snv 0.54
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.900 1.000 4 2008 2019
dbSNP: rs3129882
rs3129882
HLA-DRA
0.807 0.240 6 32441753 intron variant G/A snv 0.56
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.900 0.818 2 2010 2015
dbSNP: rs34637584
rs34637584
LRRK2
0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.900 0.996 2 2005 2020
dbSNP: rs34778348
rs34778348
LRRK2 ; LOC105369736
0.742 0.120 12 40363526 missense variant G/A snv 1.7E-03 5.8E-04
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.900 0.925 1 2006 2019
dbSNP: rs12456492
rs12456492
RIT2
0.882 0.080 18 43093415 intron variant A/G snv 0.33
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.890 0.909 1 2012 2020
dbSNP: rs11724635
rs11724635
BST1
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: rs6812193
rs6812193
FAM47E ; FAM47E-STBD1 ; LOC105377286
0.882 0.080 4 76277833 intron variant C/T snv 0.38
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.880 0.667 2 2009 2017
dbSNP: rs1564282
rs1564282
GAK
1.000 0.040 4 858525 intron variant C/T snv 8.1E-02
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.870 0.889 2 2009 2015
dbSNP: rs2736990
rs2736990
SNCA
0.882 0.080 4 89757390 intron variant G/A;T snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.860 1.000 6 2009 2018
dbSNP: rs356220
rs356220
SNCA ; LOC105377329
0.925 0.080 4 89720189 intron variant T/A;C snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.850 1.000 7 2010 2016
dbSNP: rs12817488
rs12817488
CCDC62
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: rs4698412
rs4698412
BST1
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: rs823128
rs823128
NUCKS1
1.000 0.040 1 205744250 intron variant G/A snv 0.88
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.850 1.000 2 2009 2018
dbSNP: rs823156
rs823156
SLC41A1
1.000 0.040 1 205795512 non coding transcript exon variant G/A snv 0.77 0.70
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.850 1.000 2 2011 2019
dbSNP: rs947211
rs947211
LOC105371702
0.925 0.040 1 205783537 non coding transcript exon variant A/G snv 0.64
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.840 1.000 2 2009 2017
dbSNP: rs11868035
rs11868035
SREBF1 ; RAI1
0.763 0.200 17 17811787 splice region variant G/A snv 0.45 0.33
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.840 0.500 1 2011 2019
dbSNP: rs6430538
rs6430538
CCNT2-AS1
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: rs2102808
rs2102808
LOC107985959
1.000 0.040 2 168260515 intergenic variant G/T snv 0.15
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.820 1.000 3 2011 2015
dbSNP: rs2942168
rs2942168
LINC02210 ; LINC02210-CRHR1
0.925 0.120 17 45637484 non coding transcript exon variant G/A;C;T snv 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.820 1.000 3 2011 2014
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: 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: rs11711441
rs11711441
MCCC1
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
dbSNP: rs12185268
rs12185268
SPPL2C ; MAPT-AS1
0.851 0.160 17 45846317 missense variant A/G snv 0.15 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.810 1.000 3 2011 2019
dbSNP: rs1994090
rs1994090
SLC2A13
1.000 0.040 12 40034759 intron variant G/A;T snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.810 1.000 3 2009 2016