Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs63751273 0.645 0.280 17 46010389 missense variant C/T snv 42
rs63750424 0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 30
rs63750756 0.716 0.200 17 46010324 missense variant T/G snv 2.6E-05 23
rs143624519 0.724 0.240 17 45991484 missense variant G/A;T snv 1.5E-03; 1.2E-05 17
rs63751438 0.776 0.120 17 46010388 missense variant C/T snv 16
rs1386984902
APP
0.790 0.160 21 26000095 missense variant G/A snv 9
rs63750570 0.827 0.120 17 46018629 missense variant G/A snv 8
rs63750376 0.827 0.120 17 45996657 missense variant G/T snv 7
rs63750416 0.851 0.120 17 46010373 missense variant A/C snv 7
rs63750512 0.827 0.160 17 46024010 missense variant G/A;C snv 1.2E-05 6
rs1314736087 0.851 0.120 8 109575782 frameshift variant GA/- delins 4.0E-06 5
rs63750349 0.851 0.200 17 45996638 missense variant C/G;T snv 4.0E-06 5
rs63750635 0.851 0.120 17 46014286 missense variant C/T snv 5
rs1189501362 0.882 0.120 3 119863583 missense variant G/A snv 7.0E-06 4
rs1205185774 0.882 0.120 14 77469161 missense variant C/T snv 4
rs1235948930 0.882 0.120 17 45983865 missense variant C/T snv 7.0E-06 4
rs63750129 0.882 0.120 17 45996612 missense variant A/C snv 4.0E-06 4
rs866604606 0.882 0.120 22 21772907 missense variant G/A snv 4