Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9989735
SP140
0.925 0.120 2 230250739 intron variant G/C;T snv 2
rs998592
CLEC16A
0.925 0.160 16 11105821 intron variant C/T snv 0.39 2
rs9976767
UBASH3A
0.882 0.200 21 42416281 intron variant A/G snv 0.45 3
rs9967792
STAT4
1.000 0.080 2 191109709 intron variant T/C snv 0.65 1
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs9901869 0.925 0.120 17 47497840 intergenic variant G/A snv 0.56 2
rs9891119
STAT3
0.882 0.120 17 42355962 intron variant A/C snv 0.36 3
rs987107
IL7R
1.000 0.080 5 35875125 intron variant G/A snv 0.27 1
rs9846396
ZBTB38
1.000 0.080 3 141422126 intron variant C/T snv 0.50 2
rs9828629
FOXP1
1.000 0.080 3 71481195 intron variant C/G;T snv 1
rs9828519
SLC9A9
1.000 0.080 3 143707136 intron variant G/A;C;T snv 1
rs9808753
IFNGR2
0.701 0.400 21 33415005 missense variant A/G snv 0.20 0.18 17
rs9807334 1.000 0.080 18 50997791 intron variant G/A snv 6.6E-02 2
rs9792269 0.882 0.200 8 128252343 intergenic variant A/C;G snv 5
rs9736016 1.000 0.080 11 118854185 intergenic variant T/A snv 0.41 2
rs9657904
CBLB ; LOC107986109
0.925 0.160 3 105867870 intron variant T/A;C snv 3
rs9652490
LINGO1
0.851 0.080 15 77671545 intron variant A/G snv 0.28 4
rs9596270
DLEU1
1.000 0.080 13 50268304 intron variant T/C snv 6.1E-02 1
rs9568281 1.000 0.080 13 49611068 intergenic variant A/G snv 7.5E-02 1
rs9523787
GPC5-AS1 ; GPC5
1.000 0.080 13 92711507 intron variant G/T snv 0.15 1
rs9523762
LOC105370315 ; GPC5
0.925 0.120 13 92679633 intron variant G/A snv 0.39 2
rs951005 0.807 0.200 9 34743684 intron variant G/A snv 0.78 10
rs948854
GAL ; LOC107984343
0.882 0.200 11 68682735 upstream gene variant C/T snv 0.65 4
rs947474
LINC02649 ; LINC02656
0.827 0.440 10 6348488 intron variant G/A snv 0.79 5
rs9469240 0.925 0.120 6 32722224 downstream gene variant C/T snv 0.37 2