Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs63750687
PSEN1
0.752 0.200 14 73217137 missense variant C/A;G;T snv 33
rs63750231
PSEN1
0.689 0.160 14 73198100 missense variant A/C;G snv 23
rs63750215
PSEN2
0.701 0.240 1 226885603 missense variant A/T snv 19
rs63750264
APP
0.716 0.360 21 25891784 missense variant C/A;G;T snv 17
rs63750306
PSEN1
0.701 0.320 14 73173663 missense variant A/C;G;T snv 17
rs63750083
PSEN1
0.732 0.160 14 73219177 missense variant C/A;T snv 13
rs63751287
PSEN1
0.742 0.120 14 73192792 missense variant A/G;T snv 13
rs572842823
APP
0.763 0.160 21 25897626 missense variant T/A;G snv 11
rs63750522
PSEN1
0.827 0.120 14 73173644 missense variant G/A;C snv 8
rs63750577
PSEN1
0.827 0.120 14 73186881 missense variant C/T snv 8
rs63750852
PSEN1
0.790 0.120 14 73170998 missense variant G/A;T snv 8
rs63751039
APP
0.776 0.200 21 25891855 missense variant T/C snv 8
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
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
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