Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs63750579
APP
0.742 0.280 21 25891856 missense variant C/G;T snv 13
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
rs1386984902
APP
0.790 0.160 21 26000095 missense variant G/A snv 9
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
rs63750671
APP
0.790 0.240 21 25891858 missense variant G/C snv 8
rs63750847
APP
0.790 0.120 21 25897620 missense variant C/T snv 4.5E-04 3.0E-04 8
rs63751039
APP
0.776 0.200 21 25891855 missense variant T/C snv 8
rs193922916
APP
0.827 0.080 21 25897619 missense variant G/A;C snv 6
rs950592627
APP
0.827 0.200 21 26090015 missense variant G/C snv 7.0E-06 5
rs1193124736
APP
0.851 0.120 21 25982462 missense variant G/T snv 7.0E-06 4
rs63749964
APP
0.851 0.080 21 25891783 missense variant A/C snv 4
rs63750734
APP
0.851 0.080 21 25891790 missense variant C/T snv 4
rs63750921
APP
0.882 0.200 21 25891820 missense variant G/C snv 4
rs1191863771
APP
0.925 0.080 21 25911833 missense variant A/G snv 4.0E-06 3
rs1275544322
APP
0.882 0.160 21 25975185 missense variant T/C snv 4.0E-06 7.0E-06 3
rs1281129992
APP
0.882 0.080 21 25891730 missense variant C/T snv 4.0E-06 3
rs1297968881
APP
0.882 0.200 21 26112137 missense variant C/T snv 4.0E-06 3
rs1412095491
APP
0.882 0.200 21 26051053 missense variant C/G snv 4.0E-06 3
rs199887707
APP
0.882 0.080 21 25911840 missense variant C/T snv 3.8E-04 4.9E-04 3
rs63749810
APP
0.882 0.200 21 25891853 missense variant C/T snv 3
rs63750151
APP
0.882 0.080 21 25891761 missense variant C/G;T snv 3