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: rs2316765
rs2316765
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
1.000 0.040 17 45835088 3 prime UTR variant T/C snv 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 1.000 1 2011 2011
dbSNP: rs3857053
rs3857053
SNCA
1.000 0.040 4 89724523 3 prime UTR variant C/T snv 0.24
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 1.000 1 2011 2011
dbSNP: rs4482334
rs4482334
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
1.000 0.040 17 45835464 3 prime UTR variant T/C snv 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 1.000 1 2011 2011
dbSNP: rs4640231
rs4640231
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
1.000 0.040 17 45835420 3 prime UTR variant G/A;C snv 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 1.000 1 2012 2012
dbSNP: rs878886
rs878886
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
0.925 0.080 17 45835124 3 prime UTR variant C/G;T snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 1.000 1 2012 2012
dbSNP: rs9878775
rs9878775
DCUN1D1
1.000 0.040 3 182942165 3 prime UTR variant T/A;C snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 1.000 1 2011 2011
dbSNP: rs1372519
rs1372519
SNCA ; SNCA-AS1
1.000 0.040 4 89836158 5 prime UTR variant A/G snv 0.77
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 1.000 1 2011 2011
dbSNP: rs17650901
rs17650901
MAPT
0.925 0.120 17 45962325 5 prime UTR variant A/G snv 0.14 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 1.000 1 2012 2012
dbSNP: rs199533
rs199533
NSF ; LRRC37A2
0.925 0.120 17 46751565 synonymous variant G/A snv 0.13 0.13
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.800 1.000 4 2009 2012
dbSNP: rs1052551
rs1052551
MAPT
1.000 0.040 17 45991558 synonymous variant G/A;T snv 0.14; 8.0E-05
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 1.000 1 2012 2012
dbSNP: rs1052553
rs1052553
MAPT
0.827 0.200 17 45996523 synonymous variant A/G snv 0.14 0.15
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.730 0.750 1 2010 2012
dbSNP: rs12185235
rs12185235
SPPL2C ; MAPT-AS1
0.925 0.120 17 45846337 synonymous variant C/T snv 0.14 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 1.000 1 2012 2012
dbSNP: rs17574604
rs17574604
KANSL1
0.925 0.120 17 46034247 synonymous variant A/G snv 0.15 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 1.000 1 2012 2012
dbSNP: rs17652121
rs17652121
MAPT
0.925 0.120 17 45996607 synonymous variant T/C snv 0.14 0.15
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 1.000 1 2012 2012
dbSNP: rs417968
rs417968
LINC02210 ; LINC02210-CRHR1
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: rs1981997
rs1981997
MAPT
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: 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: rs356229
rs356229
LOC105377329
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: rs393152
rs393152
LINC02210 ; LINC02210-CRHR1
0.851 0.160 17 45641777 non coding transcript exon variant A/G snv 0.18 0.29
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.810 1.000 3 2009 2015
dbSNP: rs1800547
rs1800547
MAPT
0.925 0.120 17 45974480 non coding transcript exon variant A/G snv 0.15 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.720 1.000 2 2008 2012
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: rs1396862
rs1396862
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
1.000 0.040 17 45825631 non coding transcript exon variant G/A snv 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 1.000 1 2012 2012
dbSNP: rs16940668
rs16940668
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
1.000 0.040 17 45830600 non coding transcript exon variant G/A snv 0.15 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 1.000 1 2011 2011
dbSNP: rs17763596
rs17763596
SPPL2C ; MAPT-AS1
0.925 0.120 17 45843844 non coding transcript exon variant G/T snv 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 1.000 1 2012 2012