Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs75932628 0.662 0.480 6 41161514 missense variant C/A;T snv 6.8E-05; 2.6E-03 28
rs63750215 0.701 0.240 1 226885603 missense variant A/T snv 19
rs5848 0.708 0.120 17 44352876 3 prime UTR variant C/T snv 0.41 17
rs1223904774
APP
0.790 0.120 21 25891772 missense variant C/T snv 4.0E-06 7.0E-06 8
rs72824905 0.827 0.200 16 81908423 missense variant C/G;T snv 5.2E-03 6
rs4877365 0.851 0.120 9 87540777 intron variant G/A snv 0.28 4
rs4878104 0.851 0.120 9 87578076 intron variant C/T snv 0.40 4
rs2234256 0.882 0.120 6 41158917 missense variant A/G snv 1.8E-02 4.0E-02 3