Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs61752717 0.583 0.840 16 3243407 missense variant T/A;C snv 2.8E-04 72
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs63750687 0.752 0.200 14 73217137 missense variant C/A;G;T snv 33
rs63750424 0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 30
rs75932628 0.662 0.480 6 41161514 missense variant C/A;T snv 6.8E-05; 2.6E-03 28
rs63750756 0.716 0.200 17 46010324 missense variant T/G snv 2.6E-05 23
rs1799990 0.683 0.440 20 4699605 missense variant A/G snv 0.31 0.33 23
rs63750231 0.689 0.160 14 73198100 missense variant A/C;G snv 23
rs63750215 0.701 0.240 1 226885603 missense variant A/T snv 19
rs63750264
APP
0.716 0.360 21 25891784 missense variant C/A;G;T snv 17
rs63750306 0.701 0.320 14 73173663 missense variant A/C;G;T snv 17
rs74315408 0.752 0.280 20 4699758 missense variant G/A snv 6.4E-05 4.2E-05 16
rs17125721 0.763 0.120 14 73206470 missense variant A/G snv 1.5E-02 1.5E-02 14
rs63750082 0.732 0.120 14 73192712 missense variant G/C;T snv 8.0E-06 13
rs63750083 0.732 0.160 14 73219177 missense variant C/A;T snv 13
rs63751287 0.742 0.120 14 73192792 missense variant A/G;T snv 13
rs1231783932
APP
0.763 0.120 21 26051171 missense variant T/A;C snv 1.2E-05 11
rs572842823
APP
0.763 0.160 21 25897626 missense variant T/A;G snv 11
rs371425292
APP
0.763 0.160 21 25897627 missense variant C/A;T snv 8.0E-06 10
rs63750066
APP
0.763 0.160 21 25891796 missense variant C/T snv 9.5E-05 6.3E-05 9
rs1223904774
APP
0.790 0.120 21 25891772 missense variant C/T snv 4.0E-06 7.0E-06 8
rs63751039
APP
0.776 0.200 21 25891855 missense variant T/C snv 8
rs63750522 0.827 0.120 14 73173644 missense variant G/A;C snv 8
rs63750577 0.827 0.120 14 73186881 missense variant C/T snv 8
rs63750852 0.790 0.120 14 73170998 missense variant G/A;T snv 8