Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12344615
UBQLN1
0.851 0.080 9 83666280 intron variant A/C;G snv 4
rs17563986
MAPT
1.000 0.040 17 45913906 intron variant A/G snv 0.14 4
rs17649553
MAPT
0.882 0.160 17 45917282 intron variant C/T snv 0.14 4
rs17690703
MAPT-AS1
0.882 0.160 17 45847931 intron variant C/T snv 0.18 4
rs183211
LRRC37A2 ; NSF
0.882 0.160 17 46710944 intron variant G/A snv 0.28 0.30 4
rs1876828
CRHR1 ; LINC02210-CRHR1 ; MAPT-AS1
0.851 0.160 17 45834159 intron variant C/T snv 0.14 4
rs1991556
MAPT
1.000 0.040 17 46006036 intron variant G/A snv 0.14 4
rs2074404
LRRC37A2 ; WNT3
0.925 0.120 17 46788073 intron variant T/G snv 0.27 4
rs2471738
STH ; MAPT
0.882 0.160 17 45998697 intron variant C/T snv 0.18 4
rs2736990
SNCA
0.882 0.080 4 89757390 intron variant G/A;T snv 4
rs356200
SNCA
0.882 0.160 4 89747463 intron variant T/C snv 0.44 4
rs393795
SLC6A3
0.851 0.160 5 1428399 intron variant G/T snv 0.28 4
rs441
ALDH2
0.882 0.200 12 111791045 intron variant T/C snv 0.18 4
rs466448
APP
0.925 0.040 21 26171790 intron variant A/C;G snv 4
rs4877365
DAPK1
0.851 0.120 9 87540777 intron variant G/A snv 0.28 4
rs4878104
DAPK1
0.851 0.120 9 87578076 intron variant C/T snv 0.40 4
rs4919621
PITX3
0.851 0.080 10 102238914 intron variant A/T snv 0.66 4
rs4925114
RAI1
0.925 0.080 17 17807956 intron variant A/G snv 0.53 4
rs546433642
KANSL1
0.925 0.120 17 46172742 intron variant T/C;G snv 4
rs549599956
KANSL1
0.925 0.120 17 46169798 intron variant A/G snv 4
rs894278
SNCA
0.882 0.080 4 89813384 intron variant T/G snv 0.15 4
rs9652490
LINGO1
0.851 0.080 15 77671545 intron variant A/G snv 0.28 4
rs10518765
UNC13C
1.000 0.040 15 54388434 intron variant A/C snv 0.16 3
rs1078268
STH ; MAPT
0.925 0.120 17 45998535 intron variant A/G snv 0.15 3
rs11724635
BST1
0.925 0.080 4 15735478 intron variant C/A;G snv 0.43 3