Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs372642708
APP
0.925 0.080 21 26051152 missense variant C/T snv 2.4E-05 9.8E-05 2
rs63749937
PSEN1
0.925 0.080 14 73198105 missense variant C/G;T snv 2
rs63750248
PSEN1
0.925 0.080 14 73198047 missense variant G/A;C;T snv 4.0E-06; 2.4E-05 2
rs63750322
PSEN1
0.925 0.080 14 73173654 missense variant A/G;T snv 2
rs63750569
PSEN1
0.925 0.080 14 73192711 missense variant G/A snv 2
rs63750666
PSEN2
0.925 0.080 1 226895521 missense variant C/T snv 3.6E-05 2.1E-05 2
rs63750812
PSEN2
0.925 0.080 1 226885623 missense variant G/A snv 1.6E-05 1.4E-05 2
rs63750888
PSEN1
0.925 0.080 14 73192828 missense variant A/C snv 2
rs63750963
PSEN1
0.925 0.080 14 73186884 missense variant T/C snv 2
rs63751122
APP
0.925 0.080 21 25891765 missense variant A/G snv 2
rs63751416
PSEN1
0.925 0.080 14 73217170 missense variant C/G snv 2
rs63751484
PSEN1
0.925 0.080 14 73186867 missense variant G/C snv 2
rs63751210
PSEN1
0.882 0.080 14 73186878 missense variant C/T snv 5
rs63750921
APP
0.882 0.200 21 25891820 missense variant G/C snv 4
rs63750929
PSEN1
0.882 0.080 14 73217177 missense variant G/T snv 4
rs1043202
SMUG1
0.882 0.080 12 54182178 missense variant T/A snv 3
rs121917808
PSEN1
0.882 0.080 14 73219192 missense variant C/A snv 3
rs1275544322
APP
0.882 0.160 21 25975185 missense variant T/C snv 4.0E-06 7.0E-06 3
rs63749925
PSEN1
0.882 0.080 14 73219191 missense variant C/T snv 3
rs63750265
PSEN1
0.882 0.080 14 73186869 missense variant T/A;C;G snv 3
rs63750399
APP
0.882 0.080 21 25891787 missense variant T/A;C snv 3
rs63750487
PSEN1
0.882 0.120 14 73192771 missense variant C/T snv 3
rs63750815
PSEN1
0.882 0.080 14 73170974 missense variant G/T snv 3
rs63751441
PSEN1
0.882 0.080 14 73173684 missense variant C/G;T snv 5.2E-05 3
rs772069024
APP
0.882 0.080 21 26021858 missense variant C/G;T snv 4.0E-06 3