Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs761592007
APOE
0.882 0.160 19 44909013 missense variant G/A snv 1.5E-05 4
rs779569800
APOE
1.000 0.080 19 44908714 missense variant G/A;C;T snv 1.3E-05; 6.3E-06; 6.3E-06 1
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
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
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
rs1396086494
APP
0.851 0.080 21 26051069 missense variant G/A snv 4.0E-06 6
rs193922916
APP
0.827 0.080 21 25897619 missense variant G/A;C snv 6
rs63749964
APP
0.851 0.080 21 25891783 missense variant A/C snv 4
rs1281129992
APP
0.882 0.080 21 25891730 missense variant C/T 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
rs1220355764
APP
0.925 0.080 21 26022037 missense variant T/C snv 2
rs1302192564
APP
0.925 0.080 21 26000164 missense variant G/A snv 2
rs1451944248
APP
0.925 0.080 21 25975964 missense variant G/A snv 2
rs372642708
APP
0.925 0.080 21 26051152 missense variant C/T snv 2.4E-05 9.8E-05 2
rs372702043
APP
0.925 0.120 21 25976006 missense variant G/A snv 4.0E-06 2.8E-05 2
rs63750064
APP
0.925 0.080 21 25897605 missense variant C/G;T snv 2
rs762508225
APP
0.925 0.080 21 26000044 missense variant T/G snv 4.0E-06 2
rs1307925400
APP
1.000 0.080 21 26112001 missense variant C/G;T snv 4.0E-06 1
rs1347585131
APP
1.000 0.080 21 26021974 missense variant T/C snv 4.0E-06 1