Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4402960 0.724 0.400 3 185793899 intron variant G/T snv 0.38 21
rs781049584
APP
0.724 0.280 21 26021917 missense variant T/G snv 8.2E-06 7.0E-06 18
rs1805094 0.716 0.440 1 65610269 missense variant G/C;T snv 0.16; 4.0E-06 16
rs3851179 0.752 0.280 11 86157598 downstream gene variant T/C snv 0.70 15
rs773641005 0.742 0.240 16 58723829 missense variant T/C snv 14
rs1181860747 0.776 0.240 19 7122961 missense variant C/T snv 10
rs63750526 0.776 0.160 14 73192832 missense variant C/A snv 10
rs3816873 0.790 0.200 4 99583507 missense variant T/C snv 0.25 0.26 9
rs997509 0.827 0.200 6 131846837 intron variant C/T snv 5.3E-02 6
rs2293855 0.851 0.120 8 11319901 non coding transcript exon variant G/A snv 0.35 5
rs3813929 0.851 0.240 X 114584047 upstream gene variant C/G;T snv 5
rs1527483 1.000 0.080 7 80672184 intron variant G/A snv 6.7E-02 2