Disease: Diabetes Mellitus, Insulin-Dependent
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11594656 0.776 0.240 10 6080046 intergenic variant T/A snv 0.18 9
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 13
rs2248462 0.807 0.240 6 31479019 downstream gene variant G/A snv 0.19 10
rs2516398 0.882 0.200 6 31513749 upstream gene variant G/T snv 0.70 3
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 22
rs2844494 0.925 0.160 6 31515638 upstream gene variant C/A snv 0.70 2
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
rs3129763 0.827 0.280 6 32623148 TF binding site variant G/A snv 0.23 6
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 18
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 20
rs9275312 0.807 0.280 6 32697951 intergenic variant A/G snv 0.16 6
rs9296015 0.851 0.280 6 32251212 upstream gene variant G/A snv 0.22 4
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs3733197
BANK1
0.742 0.320 4 101918130 missense variant G/A snv 0.31 0.30 13
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 18
rs763361
CD226
0.689 0.520 18 69864406 missense variant T/A;C snv 4.0E-06; 0.52 21
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs9277554
HLA-DPB1
0.790 0.520 6 33087761 3 prime UTR variant C/T snv 0.38 7
rs3129871
HLA-DRA
0.827 0.320 6 32438565 upstream gene variant A/C snv 0.59 5
rs1800587
IL1A
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs907715
IL21
0.752 0.520 4 122613898 intron variant C/T snv 0.35 11
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs12722495
IL2RA
0.851 0.200 10 6055320 intron variant T/C snv 7.0E-02 5
rs2104286
IL2RA
0.662 0.440 10 6057082 intron variant T/C snv 0.18 25