Disease: Diabetes Mellitus, Insulin-Dependent
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2844494 0.925 0.160 6 31515638 upstream gene variant C/A snv 0.70 2
rs2516398 0.882 0.200 6 31513749 upstream gene variant G/T snv 0.70 3
rs2856705 0.882 0.200 6 32703179 downstream gene variant C/T snv 0.11 3
rs3117230 0.882 0.200 6 33107858 upstream gene variant A/G snv 0.28 3
rs479536
NOTCH4
0.882 0.200 6 32225901 upstream gene variant G/A snv 5.0E-02 3
rs9296015 0.851 0.280 6 32251212 upstream gene variant G/A snv 0.22 4
rs12722495
IL2RA
0.851 0.200 10 6055320 intron variant T/C snv 7.0E-02 5
rs3129871
HLA-DRA
0.827 0.320 6 32438565 upstream gene variant A/C snv 0.59 5
rs3129763 0.827 0.280 6 32623148 TF binding site variant G/A snv 0.23 6
rs9275312 0.807 0.280 6 32697951 intergenic variant A/G snv 0.16 6
rs2516509
MICB-DT
0.882 0.160 6 31482217 intron variant T/C snv 0.19 7
rs9277554
HLA-DPB1
0.790 0.520 6 33087761 3 prime UTR variant C/T snv 0.38 7
rs11594656 0.776 0.240 10 6080046 intergenic variant T/A snv 0.18 9
rs2248462 0.807 0.240 6 31479019 downstream gene variant G/A snv 0.19 10
rs12153855
TNXB
0.776 0.320 6 32107027 intron variant T/C snv 0.11 11
rs907715
IL21
0.752 0.520 4 122613898 intron variant C/T snv 0.35 11
rs11889341
STAT4
0.732 0.480 2 191079016 intron variant C/T snv 0.21 12
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 13
rs2304256
TYK2
0.732 0.360 19 10364976 missense variant C/A snv 0.27 0.23 13
rs3733197
BANK1
0.742 0.320 4 101918130 missense variant G/A snv 0.31 0.30 13
rs1143679
ITGAM
0.732 0.520 16 31265490 missense variant G/A snv 9.7E-02 0.11 14
rs12150220
NLRP1
0.724 0.360 17 5582047 missense variant A/T snv 0.37 0.33 14
rs2670660
NLRP1
0.708 0.400 17 5615686 intron variant A/G snv 0.41 15
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 18
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 18