Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9889296 0.827 0.120 17 34243528 intergenic variant G/A snv 0.33 6
rs9868809
CELSR3
0.925 0.040 3 48643620 synonymous variant C/G;T snv 9.7E-02 3
rs9858542
BSN
0.925 0.040 3 49664550 synonymous variant G/A snv 0.26 0.27 3
rs9836291
BSN
3 49660026 intron variant G/A snv 0.30 1
rs962917
MYO9B
0.882 0.040 19 17191438 intron variant G/A snv 0.45 4
rs9557207
UBAC2
13 99384164 intron variant A/G snv 0.17 2
rs9557195
GPR183 ; UBAC2
13 99304368 intron variant T/C snv 0.16 1
rs950318 3 80354036 intergenic variant C/G snv 0.22 1
rs9471535
TREM1
0.851 0.240 6 41287752 upstream gene variant T/C snv 0.12 5
rs941823
LINC00598
0.827 0.120 13 40439840 intron variant T/C snv 0.77 6
rs9358372
CDKAL1
1.000 0.040 6 20812357 intron variant G/A snv 0.64 2
rs9313808 5 159393836 intron variant A/G snv 0.89 1
rs9297145
KPNA7
0.827 0.120 7 99161494 intergenic variant C/A snv 0.67 6
rs9282564
ABCB1
1.000 0.080 7 87600124 missense variant T/A;C;G snv 7.3E-02 7.3E-02 2
rs9271366 0.807 0.240 6 32619077 intergenic variant G/A snv 0.86 9
rs925255
FOSL2 ; FLJ31356
0.827 0.120 2 28391927 intron variant C/T snv 0.38 6
rs921720
LOC105375746
1.000 0.040 8 125522429 intron variant A/G snv 0.48 2
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 20
rs915286
LINC00598
1.000 0.040 13 40121855 intron variant G/A;C snv 2
rs913678 0.882 0.240 20 50338887 regulatory region variant T/C snv 0.51 6
rs907611
LSP1
0.882 0.160 11 1852842 upstream gene variant G/A snv 0.26 4
rs901312933
ATG16L1
0.882 0.120 2 233282746 missense variant G/A;T snv 4
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs879761216
CNR2
0.732 0.480 1 23875429 frameshift variant TT/C;T delins 14
rs878859113
CD24
0.763 0.360 6 106971734 missense variant G/A snv 0.35 11