Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1038162399
APP
0.925 0.080 21 25911954 missense variant G/A snv 4.0E-06 2
rs1200601649
APP
0.925 0.080 21 26022022 missense variant A/C snv 2
rs1231783932
APP
0.763 0.120 21 26051171 missense variant T/A;C snv 1.2E-05 11
rs1302192564
APP
0.925 0.080 21 26000164 missense variant G/A snv 2
rs1315025573
APP
0.925 0.080 21 25891849 missense variant A/C;G snv 4.0E-06 2
rs1341026713
APP
0.925 0.080 21 25955719 missense variant G/A snv 4.0E-06 1.4E-05 3
rs1396086494
APP
0.851 0.080 21 26051069 missense variant G/A snv 4.0E-06 6
rs1451944248
APP
0.925 0.080 21 25975964 missense variant G/A snv 2
rs17125721
PSEN1
0.763 0.120 14 73206470 missense variant A/G snv 1.5E-02 1.5E-02 14
rs201085152
APP
0.925 0.080 21 25975072 missense variant G/A;T snv 1.6E-05; 3.6E-05 3
rs201093867
APP
0.925 0.080 21 26021995 missense variant A/C snv 2
rs28936379
PSEN2
0.807 0.120 1 226888977 missense variant A/C;G;T snv 4.0E-06 10
rs375869205
PAM
1.000 0.080 5 103003097 missense variant C/G;T snv 1
rs571825723
PSEN1
0.925 0.080 14 73211867 missense variant C/T snv 4.4E-05 2.8E-05 4
rs61761208
PSEN2
0.882 0.080 1 226885602 missense variant A/T snv 3
rs63749806
PSEN1
0.827 0.080 14 73186902 missense variant T/C snv 7
rs63749885
PSEN1
0.882 0.080 14 73186859 missense variant C/T snv 3
rs63750001
PSEN1
0.851 0.080 14 73219188 missense variant C/T snv 4
rs63750082
PSEN1
0.732 0.120 14 73192712 missense variant G/C;T snv 8.0E-06 13
rs63750083
PSEN1
0.732 0.160 14 73219177 missense variant C/A;T snv 13
rs63750215
PSEN2
0.701 0.240 1 226885603 missense variant A/T snv 19
rs63750231
PSEN1
0.689 0.160 14 73198100 missense variant A/C;G snv 23
rs63750264
APP
0.716 0.360 21 25891784 missense variant C/A;G;T snv 17
rs63750306
PSEN1
0.701 0.320 14 73173663 missense variant A/C;G;T snv 17
rs63750424
MAPT
0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 30