Disease: Parkinson Disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs111501952
LRRK2
1.000 0.040 12 40310461 missense variant G/A snv 4.4E-05 7.7E-05 2
rs1239756674
MAOA
1.000 0.040 X 43743818 synonymous variant G/A snv 2
rs2421947
DNM3-IT1 ; DNM3
1.000 0.040 1 171863954 intron variant C/G;T snv 2
rs12817488
CCDC62
1.000 0.040 12 122811747 intron variant G/A snv 0.39 3
rs1290141855
SLC6A2
1.000 0.040 16 55698539 missense variant T/C snv 4.0E-06 7.0E-06 3
rs74315356
PINK1-AS ; PINK1
0.925 0.040 1 20649054 stop gained G/A snv 4.0E-06 1.4E-05 3
rs121918304
FBXO7
0.925 0.080 22 32498453 stop gained C/A;T snv 4.0E-06; 4.0E-06 4
rs2942168
LINC02210-CRHR1 ; LINC02210
0.925 0.120 17 45637484 non coding transcript exon variant G/A;C;T snv 0.14 4
rs368134308
PRKN
0.882 0.040 6 162443356 missense variant C/A;G;T snv 3.2E-05; 2.6E-04 4
rs71653619
PARK7
1.000 0.040 1 7970934 missense variant G/A snv 7.9E-03 7.0E-03 4
rs121917763
TH
0.925 0.040 11 2167896 missense variant A/G snv 1.2E-05 7.0E-06 5
rs201106962
SNCA
0.851 0.080 4 89828156 missense variant A/C snv 8.0E-05 7.0E-05 5
rs45539432
PINK1-AS ; PINK1
0.851 0.040 1 20649109 stop gained C/T snv 4.0E-05 3.5E-05 5
rs762472005
SACM1L
0.851 0.040 3 45722873 missense variant G/A snv 1.2E-05 7.0E-06 5
rs1224426272
CIT
0.925 0.040 12 119869138 missense variant C/T snv 6
rs387907571
DNAJC13
0.827 0.080 3 132477995 missense variant A/G snv 4.2E-06 3.5E-05 6
rs542171324
SNCA
0.851 0.160 4 89828148 missense variant G/A;C snv 8.0E-06; 4.0E-06 6
rs112176450
EIF4G1
0.807 0.080 3 184327401 missense variant G/A;T snv 2.1E-04 2.8E-04 7
rs34995376
LRRK2
0.807 0.080 12 40310435 missense variant G/A snv 7.0E-06 7
rs35801418
LRRK2
0.827 0.120 12 40321114 missense variant A/G snv 7
rs34015634
LRRK2
0.851 0.120 12 40340380 missense variant T/C snv 3.2E-05 1.4E-05 8
rs774005786
PARK7
0.790 0.080 1 7970951 missense variant G/A;T snv 3.9E-04; 2.0E-05 8
rs188286943
VPS35
0.776 0.160 16 46662452 missense variant C/T snv 9
rs113994099
POLG
0.827 0.240 15 89320883 missense variant T/C snv 10
rs767543900
MAPT
0.790 0.120 17 45971879 missense variant A/C;G snv 4.0E-06 10