Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs80356702 0.882 0.120 7 143330868 missense variant G/A snv 4.0E-06 1.4E-05 9
rs767543900 0.790 0.120 17 45971879 missense variant A/C;G snv 4.0E-06 10
rs1163944538 0.641 0.560 17 75494905 frameshift variant -/A delins 4.0E-06 73
rs1397094538 0.925 0.120 1 23367044 missense variant A/T snv 4.0E-06 3
rs713041 0.776 0.400 19 1106616 stop gained T/A;C snv 4.2E-06; 0.58 16
rs555145190 0.732 0.360 17 42543921 stop gained G/A;C;T snv 4.2E-06 21
rs1424266770 0.790 0.200 4 184632307 missense variant C/G snv 8.0E-06 10
rs775129479 0.851 0.120 16 1791387 missense variant G/A;C;T snv 1.6E-05; 8.1E-06; 8.1E-06 6
rs781049584
APP
0.724 0.280 21 26021917 missense variant T/G snv 8.2E-06 7.0E-06 18
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs763868966 1.000 0.080 17 44911429 stop gained C/A;G;T snv 1.2E-05; 4.0E-05 4
rs63750424 0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 30
rs781587642 0.851 0.120 2 219250557 missense variant G/A;C snv 2.0E-05 6
rs148881970 0.724 0.360 17 42543840 missense variant A/G snv 5.4E-05 1.3E-04 22
rs74315408 0.752 0.280 20 4699758 missense variant G/A snv 6.4E-05 4.2E-05 16
rs768823392 0.827 0.120 16 89546657 coding sequence variant GGCGGGAGA/- delins 2.6E-04 4.2E-04 10
rs104894396 0.672 0.400 13 20189511 stop gained C/T snv 5.8E-04 1.1E-04 28
rs28937900 0.752 0.160 19 46756276 missense variant C/A;T snv 1.0E-03 37
rs17125721 0.763 0.120 14 73206470 missense variant A/G snv 1.5E-02 1.5E-02 14
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs6277 0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38 36
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249