Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2391191
DAOA-AS1 ; DAOA
0.807 0.080 13 105467097 missense variant G/A snv 0.40 0.32 7
rs63749806
PSEN1
0.827 0.080 14 73186902 missense variant T/C snv 7
rs63750599
PSEN1
0.827 0.160 14 73170963 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
rs765670175
PSEN1
0.790 0.120 14 73173646 missense variant T/A snv 8.0E-06 7
rs1396086494
APP
0.851 0.080 21 26051069 missense variant G/A snv 4.0E-06 6
rs63750646
PSEN1
0.807 0.120 14 73217147 missense variant G/C snv 6
rs63750730
PSEN1
0.827 0.120 14 73173574 missense variant C/T snv 6
rs63751235
PSEN1
0.807 0.120 14 73198117 missense variant C/G snv 6
rs140501902
PSEN2
0.807 0.160 1 226883774 missense variant C/T snv 3.6E-03 3.4E-03 6
rs1057518919
PSEN1
0.851 0.120 14 73171023 missense variant T/G snv 5
rs63749835
PSEN1
0.851 0.080 14 73192799 missense variant T/C snv 5
rs63749891
PSEN1
0.851 0.080 14 73198094 missense variant G/C;T snv 5
rs63750009
PSEN1
0.851 0.120 14 73192760 missense variant A/C;G snv 5
rs63751106
PSEN1
0.827 0.080 14 73173643 missense variant T/A;C snv 5
rs63751210
PSEN1
0.882 0.080 14 73186878 missense variant C/T snv 5
rs533813519
PSEN2
0.851 0.120 1 226888097 missense variant C/A snv 1.9E-04 4.2E-05 5
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
rs63750929
PSEN1
0.882 0.080 14 73217177 missense variant G/T snv 4
rs63751254
PSEN1
0.851 0.160 14 73217210 missense variant A/G snv 4
rs1191863771
APP
0.925 0.080 21 25911833 missense variant A/G snv 4.0E-06 3