Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs63749964
APP
0.851 0.080 21 25891783 missense variant A/C snv 4
rs63750524
PSEN1
1.000 0.080 14 73198095 missense variant A/C snv 2
rs63750888
PSEN1
0.925 0.080 14 73192828 missense variant A/C snv 2
rs63750110
PSEN2
1.000 0.080 1 226895548 missense variant A/C snv 3.6E-05 3.5E-05 1
rs63751320
PSEN1
1.000 0.080 14 73192862 missense variant A/C snv 1
rs63750231
PSEN1
0.689 0.160 14 73198100 missense variant A/C;G snv 23
rs63750009
PSEN1
0.851 0.120 14 73192760 missense variant A/C;G snv 5
rs747363386
PSEN1
1.000 0.080 14 73173669 missense variant A/C;G snv 8.0E-06 1
rs63750306
PSEN1
0.701 0.320 14 73173663 missense variant A/C;G;T snv 17
rs1799990
PRNP
0.683 0.440 20 4699605 missense variant A/G snv 0.31 0.33 23
rs17125721
PSEN1
0.763 0.120 14 73206470 missense variant A/G snv 1.5E-02 1.5E-02 14
rs63751037
PSEN1
0.790 0.080 14 73173642 missense variant A/G snv 7
rs63751254
PSEN1
0.851 0.160 14 73217210 missense variant A/G snv 4
rs1191863771
APP
0.925 0.080 21 25911833 missense variant A/G snv 4.0E-06 3
rs63751122
APP
0.925 0.080 21 25891765 missense variant A/G snv 2
rs63751287
PSEN1
0.742 0.120 14 73192792 missense variant A/G;T snv 13
rs63750322
PSEN1
0.925 0.080 14 73173654 missense variant A/G;T snv 2
rs63750215
PSEN2
0.701 0.240 1 226885603 missense variant A/T snv 19
rs1426802434
BIN1
1.000 0.080 2 127070588 missense variant A/T snv 4.0E-06 1
rs923630119
TMEM106B
1.000 0.080 7 12215024 missense variant A/T snv 1
rs533813519
PSEN2
0.851 0.120 1 226888097 missense variant C/A snv 1.9E-04 4.2E-05 5
rs121917808
PSEN1
0.882 0.080 14 73219192 missense variant C/A snv 3
rs63750687
PSEN1
0.752 0.200 14 73217137 missense variant C/A;G;T snv 33
rs63750264
APP
0.716 0.360 21 25891784 missense variant C/A;G;T snv 17
rs75932628
LOC105375056 ; TREM2
0.662 0.480 6 41161514 missense variant C/A;T snv 6.8E-05; 2.6E-03 28