Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs63750424 0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 30
rs63750215 0.701 0.240 1 226885603 missense variant A/T snv 19
rs781049584
APP
0.724 0.280 21 26021917 missense variant T/G snv 8.2E-06 7.0E-06 18
rs63750264
APP
0.716 0.360 21 25891784 missense variant C/A;G;T snv 17
rs3091244
CRP
0.724 0.280 1 159714875 upstream gene variant G/A;T snv 17
rs2794521
CRP
0.742 0.480 1 159715306 upstream gene variant C/T snv 0.78 15
rs63750579
APP
0.742 0.280 21 25891856 missense variant C/G;T snv 13
rs74315409 0.742 0.240 20 4699915 missense variant T/G snv 6.0E-05 2.1E-05 13
rs1035071612 0.763 0.240 19 11113361 missense variant C/A;T snv 4.0E-06 9
rs63750671
APP
0.790 0.240 21 25891858 missense variant G/C snv 8
rs63750311 0.790 0.240 14 73192647 missense variant A/C snv 8
rs63750522 0.827 0.120 14 73173644 missense variant G/A;C snv 8
rs765670175 0.790 0.120 14 73173646 missense variant T/A snv 8.0E-06 7
rs3093075 0.882 0.120 1 159710123 upstream gene variant G/T snv 0.13 5
rs79524815 0.851 0.240 7 18658708 intron variant T/G snv 3.8E-02 4
rs34487851 0.882 0.200 2 106026098 regulatory region variant A/G snv 0.28 3
rs1412095491
APP
0.882 0.200 21 26051053 missense variant C/G snv 4.0E-06 3
rs6910730 0.925 0.080 6 41278895 intron variant A/G snv 0.21 3
rs191838178 0.925 0.160 22 40407449 missense variant C/T snv 2.4E-05 7.0E-06 2
rs10908821 1.000 0.040 1 161038745 intron variant C/G snv 0.11 1
rs2774276 1.000 0.040 1 161041926 intron variant G/A;C snv 1