Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs367709245
APP
1.000 0.080 21 25891634 intron variant TACTTA/- delins 2.3E-03 1
rs63750756
MAPT
0.716 0.200 17 46010324 missense variant T/G snv 2.6E-05 23
rs63750802
PSEN1
0.851 0.080 14 73219144 missense variant T/G snv 7
rs1057518919
PSEN1
0.851 0.120 14 73171023 missense variant T/G snv 5
rs63749961
PSEN1
0.925 0.080 14 73192772 missense variant T/G snv 3
rs1179768627
PSEN1
0.925 0.080 14 73198064 missense variant T/G snv 4.0E-06 2
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
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
rs63749835
PSEN1
0.851 0.080 14 73192799 missense variant T/C snv 5
rs1275544322
APP
0.882 0.160 21 25975185 missense variant T/C snv 4.0E-06 7.0E-06 3
rs63750963
PSEN1
0.925 0.080 14 73186884 missense variant T/C snv 2
rs572842823
APP
0.763 0.160 21 25897626 missense variant T/A;G snv 11
rs63751032
PSEN1
0.851 0.080 14 73219156 missense variant T/A;G snv 7
rs63750265
PSEN1
0.882 0.080 14 73186869 missense variant T/A;C;G snv 3
rs61752717
MEFV
0.583 0.840 16 3243407 missense variant T/A;C snv 2.8E-04 72
rs1231783932
APP
0.763 0.120 21 26051171 missense variant T/A;C snv 1.2E-05 11
rs63751106
PSEN1
0.827 0.080 14 73173643 missense variant T/A;C snv 5
rs63750399
APP
0.882 0.080 21 25891787 missense variant T/A;C snv 3
rs765670175
PSEN1
0.790 0.120 14 73173646 missense variant T/A snv 8.0E-06 7
rs1043202
SMUG1
0.882 0.080 12 54182178 missense variant T/A snv 3
rs63750588
PSEN1
0.925 0.080 14 73173687 missense variant T/A snv 3
rs63750929
PSEN1
0.882 0.080 14 73217177 missense variant G/T snv 4
rs63750815
PSEN1
0.882 0.080 14 73170974 missense variant G/T snv 3