Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs63750416
MAPT
0.851 0.120 17 46010373 missense variant A/C snv 7
rs63750129
MAPT
0.882 0.120 17 45996612 missense variant A/C snv 4.0E-06 4
rs886039227
DCTN1
0.925 0.200 2 74378123 missense variant A/C snv 4
rs760073870
CAPN2
1 223752954 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 1
rs776045205
CAST
5 96747369 missense variant C/A;T snv 6.4E-05; 2.4E-04 1
rs63750349
MAPT
0.851 0.200 17 45996638 missense variant C/G;T snv 4.0E-06 5
rs1348073540
ARHGAP22 ; MAPK8
10 48431259 missense variant C/G;T snv 4.0E-06 1
rs752410089
CAST
5 96741548 missense variant C/G;T 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
rs63750635
MAPT
0.851 0.120 17 46014286 missense variant C/T snv 5
rs1205185774
AHSA1
0.882 0.120 14 77469161 missense variant C/T snv 4
rs1235948930
MAPT
0.882 0.120 17 45983865 missense variant C/T snv 7.0E-06 4
rs763872192
CD36
0.882 0.080 7 80672000 missense variant C/T snv 2.8E-05 4
rs1235134025
CAST
5 96740769 missense variant C/T snv 4.0E-06 1
rs1411928276
DCT
13 94479251 missense variant C/T snv 1
rs376388064
VEGFA
6 43782006 missense variant C/T snv 2.8E-05 3.5E-05 1
rs775645890
UPK3B
7 76515192 missense variant C/T snv 1
rs779612015
UPK3B
7 76515186 missense variant C/T snv 4.7E-06 1
rs780325052
CAST
5 96746417 missense variant C/T snv 2.0E-05 3.5E-05 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