Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs482541
LOC107983981
1.000 0.120 15 53216997 intergenic variant A/G snv 0.81 1
rs3129888
HLA-DRA
0.882 0.240 6 32443949 intron variant G/A snv 0.82 0.80 4
rs8007115 1.000 0.120 14 94871151 intergenic variant T/C snv 0.80 1
rs2247056
LOC112267902 ; HLA-B ; LINC02571
0.882 0.160 6 31297713 intron variant T/C snv 0.80 11
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 18
rs7773694 0.882 0.280 6 32738557 upstream gene variant A/G snv 0.80 3
rs7755596 0.882 0.280 6 32738701 upstream gene variant C/T snv 0.80 3
rs3135002 1.000 0.120 6 32700662 TF binding site variant A/C snv 0.80 2
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs947474
LINC02649 ; LINC02656
0.827 0.440 10 6348488 intron variant G/A snv 0.79 5
rs10181656
STAT4
0.763 0.360 2 191105153 intron variant G/C snv 0.79 9
rs2075184 0.724 0.240 2 102464132 intergenic variant T/C snv 0.78 14
rs822342
CD274
1.000 0.120 9 5453973 intron variant T/C snv 0.78 1
rs1217412
AP4B1-AS1 ; PTPN22
1.000 0.120 1 113814589 3 prime UTR variant G/A snv 0.78 1
rs2395182
HLA-DRA
0.851 0.280 6 32445540 downstream gene variant G/T snv 0.76 5
rs3448
GPX1 ; RHOA
0.776 0.240 3 49359318 3 prime UTR variant T/C snv 0.76 8
rs2596472
HCP5
1.000 0.120 6 31461190 intron variant G/A snv 0.76 1
rs910049
TSBP1-AS1 ; TSBP1
0.776 0.400 6 32347950 intron variant T/C snv 0.76 8
rs11160219 1.000 0.120 14 94869154 regulatory region variant A/G snv 0.75 1
rs2107202
TRIM40
1.000 0.120 6 30137966 intron variant T/C snv 0.75 2
rs2844533 0.925 0.200 6 31383025 upstream gene variant G/A snv 0.74 2
rs1419675 1.000 0.120 6 30124930 intergenic variant G/T snv 0.74 2
rs3130617
BAG6 ; C6orf47
0.925 0.200 6 31659746 missense variant C/T snv 0.79 0.74 2
rs9276162 0.882 0.280 6 32730680 downstream gene variant G/A snv 0.74 3
rs3132131 1.000 0.120 6 32931708 downstream gene variant A/G snv 0.73 1