Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs63750756
MAPT
0.716 0.200 17 46010324 missense variant T/G snv 2.6E-05 23
rs1314736087
SYBU
0.851 0.120 8 109575782 frameshift variant GA/- delins 4.0E-06 5
rs63750376
MAPT
0.827 0.120 17 45996657 missense variant G/T snv 7
rs143624519
MAPT
0.724 0.240 17 45991484 missense variant G/A;T snv 1.5E-03; 1.2E-05 17
rs281860580
HLA-B ; HLA-C
6 31270083 missense variant G/A;T snv 1
rs769483065
HSP90AA1
14 102085426 missense variant G/A;T snv 8.0E-06 1
rs63750512
MAPT
0.827 0.160 17 46024010 missense variant G/A;C snv 1.2E-05 6
rs201792381
APP
1.000 0.080 21 25997384 missense variant G/A;C snv 1.6E-05 2
rs768194029
NFATC2
20 51523286 missense variant G/A;C snv 4.0E-06 1
rs34637584
LRRK2
0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs242557
MAPT
0.752 0.200 17 45942346 intron variant G/A snv 0.36 12
rs1386984902
APP
0.790 0.160 21 26000095 missense variant G/A snv 9
rs63750570
MAPT
0.827 0.120 17 46018629 missense variant G/A snv 8
rs1189501362
GSK3B
0.882 0.120 3 119863583 missense variant G/A snv 7.0E-06 4
rs866604606
MAPK1
0.882 0.120 22 21772907 missense variant G/A snv 4
rs587778556
NFE2L2
2 177231705 missense variant G/A snv 3.2E-05 4.9E-05 2
rs755135182
NFE2L2
2 177231657 missense variant G/A snv 4.0E-06 2
rs1005752506
AMPH
7 38461398 missense variant G/A snv 7.0E-06 1
rs1300858963
OGA
10 101799033 missense variant G/A snv 4.0E-06 1
rs1424794503
MFGE8
15 88899478 missense variant G/A snv 8.0E-06 1
rs893595382
DLG4
17 7196908 missense variant G/A snv 4.0E-06 7.0E-06 1
rs63751273
MAPT
0.645 0.280 17 46010389 missense variant C/T snv 42
rs63750424
MAPT
0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 30
rs63751438
MAPT
0.776 0.120 17 46010388 missense variant C/T snv 16
rs398122403
SYNJ1
0.807 0.080 21 32695106 missense variant C/T snv 1.2E-05 11