Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs63750264
APP
0.716 0.360 21 25891784 missense variant C/A;G;T snv 17
rs1231783932
APP
0.763 0.120 21 26051171 missense variant T/A;C snv 1.2E-05 11
rs572842823
APP
0.763 0.160 21 25897626 missense variant T/A;G snv 11
rs371425292
APP
0.763 0.160 21 25897627 missense variant C/A;T snv 8.0E-06 10
rs63750066
APP
0.763 0.160 21 25891796 missense variant C/T snv 9.5E-05 6.3E-05 9
rs1223904774
APP
0.790 0.120 21 25891772 missense variant C/T snv 4.0E-06 7.0E-06 8
rs63751039
APP
0.776 0.200 21 25891855 missense variant T/C snv 8
rs1396086494
APP
0.851 0.080 21 26051069 missense variant G/A snv 4.0E-06 6
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
rs1191863771
APP
0.925 0.080 21 25911833 missense variant A/G snv 4.0E-06 3
rs1275544322
APP
0.882 0.160 21 25975185 missense variant T/C snv 4.0E-06 7.0E-06 3
rs63750399
APP
0.882 0.080 21 25891787 missense variant T/A;C snv 3
rs772069024
APP
0.882 0.080 21 26021858 missense variant C/G;T snv 4.0E-06 3
rs200347552
APP
0.925 0.080 21 26090000 missense variant G/A snv 1.6E-05 3.5E-05 2
rs372642708
APP
0.925 0.080 21 26051152 missense variant C/T snv 2.4E-05 9.8E-05 2
rs63751122
APP
0.925 0.080 21 25891765 missense variant A/G snv 2
rs1208508997
APP
1.000 0.080 21 26051097 missense variant G/C snv 4.0E-06 1
rs367709245
APP
1.000 0.080 21 25891634 intron variant TACTTA/- delins 2.3E-03 1
rs749453173
APP
1.000 0.080 21 25997360 missense variant G/A;C snv 4.0E-06; 4.0E-06 1
rs1426802434
BIN1
1.000 0.080 2 127070588 missense variant A/T snv 4.0E-06 1
rs2391191
DAOA-AS1 ; DAOA
0.807 0.080 13 105467097 missense variant G/A snv 0.40 0.32 7
rs543578531
GRN
1.000 0.080 17 44349703 missense variant C/A;T snv 2.3E-04; 8.0E-06 1