Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs958576773
ITPR3
1.000 0.080 6 33662534 missense variant G/A snv 1
rs866914724
PSEN1
0.882 0.080 14 73173685 missense variant T/C snv 3
rs781049584
APP
0.724 0.280 21 26021917 missense variant T/G snv 8.2E-06 7.0E-06 18
rs779569800
APOE
1.000 0.080 19 44908714 missense variant G/A;C;T snv 1.3E-05; 6.3E-06; 6.3E-06 1
rs779407819
APP
1.000 0.080 21 26021899 missense variant G/A snv 1.6E-05 1
rs779296437
PSEN1
0.925 0.080 14 73192699 missense variant A/T snv 4.0E-06 2
rs778936527
PSEN2
0.925 0.080 1 226885669 missense variant G/A snv 2.4E-05 7.0E-06 2
rs773029808
SORBS2
1.000 0.080 4 185626897 missense variant C/G snv 2.0E-05 1
rs769757835
APP
1.000 0.080 21 26000117 missense variant C/T snv 4.0E-06 1
rs765670175
PSEN1
0.790 0.120 14 73173646 missense variant T/A snv 8.0E-06 7
rs762508225
APP
0.925 0.080 21 26000044 missense variant T/G snv 4.0E-06 2
rs761592007
APOE
0.882 0.160 19 44909013 missense variant G/A snv 1.5E-05 4
rs661
PSEN1
0.807 0.120 14 73217225 missense variant G/A;T snv 4.0E-06 6
rs63751441
PSEN1
0.882 0.080 14 73173684 missense variant C/G;T snv 5.2E-05 3
rs63751420
PSEN1
0.925 0.080 14 73198040 missense variant C/T snv 2
rs63751309
PSEN1
0.882 0.080 14 73192733 missense variant T/C snv 3
rs63751235
PSEN1
0.807 0.120 14 73198117 missense variant C/G snv 6
rs63751163
PSEN1
0.807 0.120 14 73192844 missense variant T/C snv 7
rs63751141
PSEN1
0.882 0.080 14 73170984 missense variant G/C snv 3
rs63751106
PSEN1
0.827 0.080 14 73173643 missense variant T/A;C snv 5
rs63751039
APP
0.776 0.200 21 25891855 missense variant T/C snv 8
rs63751037
PSEN1
0.790 0.080 14 73173642 missense variant A/G snv 7
rs63751032
PSEN1
0.851 0.080 14 73219156 missense variant T/A;G snv 7
rs63750907
PSEN1
0.807 0.120 14 73173667 missense variant C/T snv 6
rs63750900
PSEN1
0.763 0.160 14 73198067 missense variant G/A snv 4.0E-06 7.0E-06 9