Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs572842823
APP
0.763 0.160 21 25897626 missense variant T/A;G snv 11
rs63750526
PSEN1
0.776 0.160 14 73192832 missense variant C/A snv 10
rs63750590
PSEN1
0.790 0.120 14 73186860 missense variant A/G snv 10
rs63750311
PSEN1
0.790 0.240 14 73192647 missense variant A/C snv 8
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
rs10524523
TOMM40
0.807 0.200 19 44899792 intron variant TTTTTTTTTTTTTTTTTTTTTTT/-;T;TT;TTT;TTTT;TTTTT;TTTTTT;TTTTTTT;TTTTTTTT;TTTTTTTTT;TTTTTTTTTT;TTTTTTTTTTT;TTTTTTTTTTTT;TTTTTTTTTTTTT;TTTTTTTTTTTTTT;TTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT delins 7
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
rs63751163
PSEN1
0.807 0.120 14 73192844 missense variant T/C snv 7
rs193922916
APP
0.827 0.080 21 25897619 missense variant G/A;C snv 6
rs63749805
PSEN1
0.807 0.120 14 73173577 missense variant C/G;T snv 6
rs63750730
PSEN1
0.827 0.120 14 73173574 missense variant C/T snv 6
rs63750907
PSEN1
0.807 0.120 14 73173667 missense variant C/T snv 6
rs63751235
PSEN1
0.807 0.120 14 73198117 missense variant C/G snv 6
rs63749884
PSEN2
0.851 0.160 1 226888979 missense variant G/A snv 5