Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1038162399
APP
0.925 0.080 21 25911954 missense variant G/A snv 4.0E-06 2
rs1041833271
APP
0.925 0.080 21 25975995 missense variant C/T snv 7.0E-06 2
rs113145702
APP
1.000 0.080 21 25955632 missense variant A/G snv 1
rs1183474845
APP
1.000 0.080 21 26053328 missense variant C/T snv 8.0E-06 1
rs1191863771
APP
0.925 0.080 21 25911833 missense variant A/G snv 4.0E-06 3
rs1193124736
APP
0.851 0.120 21 25982462 missense variant G/T snv 7.0E-06 4
rs1200601649
APP
0.925 0.080 21 26022022 missense variant A/C snv 2
rs1220355764
APP
0.925 0.080 21 26022037 missense variant T/C snv 2
rs1223904774
APP
0.790 0.120 21 25891772 missense variant C/T snv 4.0E-06 7.0E-06 8
rs1224230940
APP
1.000 0.080 21 26053304 missense variant T/C snv 4.0E-06 1
rs1260168075
APP
1.000 0.080 21 25975217 missense variant C/G snv 1
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
rs1287723181
APP
1.000 0.080 21 25954680 missense variant G/A;C snv 4.0E-06; 4.0E-06 2
rs1297968881
APP
0.882 0.200 21 26112137 missense variant C/T snv 4.0E-06 3
rs1315025573
APP
0.925 0.080 21 25891849 missense variant A/C;G snv 4.0E-06 2
rs1386984902
APP
0.790 0.160 21 26000095 missense variant G/A snv 9
rs1412095491
APP
0.882 0.200 21 26051053 missense variant C/G snv 4.0E-06 3
rs1468425505
APP
1.000 0.080 21 26022019 missense variant G/A snv 4.0E-06 1
rs193922916
APP
0.827 0.080 21 25897619 missense variant G/A;C snv 6
rs199887707
APP
0.882 0.080 21 25911840 missense variant C/T snv 3.8E-04 4.9E-04 3
rs200074159
APP
0.925 0.080 21 26000036 missense variant T/C snv 2.8E-05 5.6E-05 2
rs200347552
APP
0.925 0.080 21 26090000 missense variant G/A snv 1.6E-05 3.5E-05 2
rs200396597
APP
1.000 0.080 21 25881743 missense variant C/T snv 7.0E-06 2
rs200620364
APP
0.925 0.080 21 26021849 missense variant C/T snv 2