Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs201093867
APP
0.925 0.080 21 26021995 missense variant A/C snv 2
rs201732035
APP
1.000 0.080 21 26021924 missense variant G/A;T snv 4.1E-06 1
rs201792381
APP
1.000 0.080 21 25997384 missense variant G/A;C snv 1.6E-05 2
rs202218688
APP
1.000 0.080 21 26000131 missense variant C/A;T snv 4.0E-06; 5.6E-05 2
rs281865161
APP
0.925 0.080 21 25897626 missense variant TC/GA mnv 2
rs2830077
APP
1.000 0.080 21 26130406 intron variant C/A snv 0.38 1
rs364048
APP
1.000 0.080 21 26171723 intron variant T/C snv 8.4E-02 1
rs371425292
APP
0.763 0.160 21 25897627 missense variant C/A;T snv 8.0E-06 10
rs466433
APP
1.000 0.080 21 26171645 intron variant A/G snv 8.3E-02 1
rs572842823
APP
0.763 0.160 21 25897626 missense variant T/A;G snv 11
rs63749810
APP
0.882 0.200 21 25891853 missense variant C/T snv 3
rs63749964
APP
0.851 0.080 21 25891783 missense variant A/C snv 4
rs63750064
APP
0.925 0.080 21 25897605 missense variant C/G;T snv 2
rs63750066
APP
0.763 0.160 21 25891796 missense variant C/T snv 9.5E-05 6.3E-05 9
rs63750151
APP
0.882 0.080 21 25891761 missense variant C/G;T snv 3
rs63750264
APP
0.716 0.360 21 25891784 missense variant C/A;G;T snv 17
rs63750399
APP
0.882 0.080 21 25891787 missense variant T/A;C snv 3
rs63750579
APP
0.742 0.280 21 25891856 missense variant C/G;T snv 13
rs63750643
APP
0.882 0.080 21 25891793 missense variant T/C snv 3
rs63750671
APP
0.790 0.240 21 25891858 missense variant G/C snv 8
rs63750734
APP
0.851 0.080 21 25891790 missense variant C/T snv 4
rs63750847
APP
0.790 0.120 21 25897620 missense variant C/T snv 4.5E-04 3.0E-04 8
rs63750921
APP
0.882 0.200 21 25891820 missense variant G/C snv 4
rs63750973
APP
0.882 0.120 21 25891792 missense variant G/A snv 3
rs63751039
APP
0.776 0.200 21 25891855 missense variant T/C snv 8