Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs63749806
PSEN1
0.827 0.080 14 73186902 missense variant T/C snv 7
rs63750802
PSEN1
0.851 0.080 14 73219144 missense variant T/G snv 7
rs63751032
PSEN1
0.851 0.080 14 73219156 missense variant T/A;G snv 7
rs63751037
PSEN1
0.790 0.080 14 73173642 missense variant A/G snv 7
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
rs28936380
PSEN2
0.827 0.080 1 226885546 missense variant C/G;T snv 1.2E-05 5
rs63751106
PSEN1
0.827 0.080 14 73173643 missense variant T/A;C snv 5
rs63749964
APP
0.851 0.080 21 25891783 missense variant A/C snv 4
rs63750001
PSEN1
0.851 0.080 14 73219188 missense variant C/T snv 4
rs121917808
PSEN1
0.882 0.080 14 73219192 missense variant C/A snv 3
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
rs58973334
PSEN2
0.882 0.080 1 226883748 missense variant G/A snv 8.6E-03 1.4E-02 3
rs63750601
PSEN1
0.882 0.080 14 73170995 missense variant G/T snv 3
rs63751141
PSEN1
0.882 0.080 14 73170984 missense variant G/C snv 3
rs63751309
PSEN1
0.882 0.080 14 73192733 missense variant T/C snv 3
rs63751441
PSEN1
0.882 0.080 14 73173684 missense variant C/G;T snv 5.2E-05 3
rs866914724
PSEN1
0.882 0.080 14 73173685 missense variant T/C snv 3
rs115865530
PSEN1
0.925 0.080 14 73206449 missense variant A/G snv 1.4E-04 4.2E-05 2
rs1179768627
PSEN1
0.925 0.080 14 73198064 missense variant T/G snv 4.0E-06 2
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