Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs950592627
APP
0.827 0.200 21 26090015 missense variant G/C snv 7.0E-06 5
rs781215285
APP
1.000 0.080 21 26051030 missense variant C/G snv 4.0E-06 1
rs781049584
APP
0.724 0.280 21 26021917 missense variant T/G snv 8.2E-06 7.0E-06 18
rs778758780
APP
1.000 0.080 21 25975137 missense variant A/G snv 8.0E-06 1
rs777260127
APP
1.000 0.080 21 26089993 missense variant C/T snv 1.6E-05 4.9E-05 1
rs772069024
APP
0.882 0.080 21 26021858 missense variant C/G;T snv 4.0E-06 3
rs772020679
APP
1.000 0.080 21 26053285 missense variant C/G snv 4.0E-06 7.0E-06 1
rs763852444
APP
0.882 0.120 21 26112127 missense variant G/C snv 4.0E-06 3
rs762508225
APP
0.925 0.080 21 26000044 missense variant T/G snv 4.0E-06 2
rs755525590
APP
1.000 0.080 21 26051028 missense variant C/T snv 1.2E-05 7.0E-06 1
rs63751122
APP
0.925 0.080 21 25891765 missense variant A/G snv 2
rs63751039
APP
0.776 0.200 21 25891855 missense variant T/C snv 8
rs63750973
APP
0.882 0.120 21 25891792 missense variant G/A snv 3
rs63750921
APP
0.882 0.200 21 25891820 missense variant G/C snv 4
rs63750847
APP
0.790 0.120 21 25897620 missense variant C/T snv 4.5E-04 3.0E-04 8
rs63750734
APP
0.851 0.080 21 25891790 missense variant C/T snv 4
rs63750671
APP
0.790 0.240 21 25891858 missense variant G/C snv 8
rs63750643
APP
0.882 0.080 21 25891793 missense variant T/C snv 3
rs63750579
APP
0.742 0.280 21 25891856 missense variant C/G;T snv 13
rs63750399
APP
0.882 0.080 21 25891787 missense variant T/A;C snv 3
rs63750264
APP
0.716 0.360 21 25891784 missense variant C/A;G;T snv 17
rs63750151
APP
0.882 0.080 21 25891761 missense variant C/G;T snv 3
rs63750066
APP
0.763 0.160 21 25891796 missense variant C/T snv 9.5E-05 6.3E-05 9
rs63750064
APP
0.925 0.080 21 25897605 missense variant C/G;T snv 2
rs63749964
APP
0.851 0.080 21 25891783 missense variant A/C snv 4