Disease: Diabetes Mellitus, Insulin-Dependent
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10181656
STAT4
0.763 0.360 2 191105153 intron variant G/C snv 0.79 9
rs10484566
PSMB9
0.925 0.200 6 32867481 regulatory region variant T/G snv 6.8E-02 2
rs1055569
HCG26 ; HCP5
0.882 0.240 6 31472305 non coding transcript exon variant C/T snv 0.41 3
rs1077393
BAG6
0.882 0.200 6 31642752 non coding transcript exon variant A/G snv 0.44 3
rs10795791 0.925 0.200 10 6066377 upstream gene variant A/G snv 0.40 2
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs11203203
UBASH3A
0.807 0.240 21 42416077 intron variant G/A snv 0.28 9
rs11889341
STAT4
0.732 0.480 2 191079016 intron variant C/T snv 0.21 12
rs1214611
CD247
0.925 0.200 1 167479867 intron variant A/G snv 0.54 2
rs12153855
TNXB
0.776 0.320 6 32107027 intron variant T/C snv 0.11 11
rs12177980
LOC102725019
0.925 0.200 6 32718307 non coding transcript exon variant G/A snv 0.37 2
rs12198173
TNXB
0.827 0.240 6 32059031 intron variant G/A snv 0.10 9
rs12566340
AP4B1-AS1 ; BCL2L15
0.925 0.200 1 113877706 3 prime UTR variant C/A;T snv 3
rs12660382
HCP5
0.882 0.200 6 31475546 intron variant C/T snv 0.19 3
rs12708716
CLEC16A
0.807 0.320 16 11086016 intron variant A/G snv 0.37 7
rs1270942
CFB ; CYP21A2
0.742 0.440 6 31951083 non coding transcript exon variant A/G snv 7.5E-02 11
rs12917716
CLEC16A
0.851 0.200 16 11095291 intron variant G/C snv 0.51 4
rs13199524
TNXB
0.807 0.240 6 32098988 intron variant C/T snv 8.4E-02 9
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 18
rs1480380
HLA-DMB
0.763 0.360 6 32945469 intron variant C/T snv 0.11 10
rs154981 0.925 0.200 6 32913216 regulatory region variant C/A;G;T snv 2
rs1678542
KIF5A
0.790 0.320 12 57574932 intron variant C/G snv 0.42 9
rs1738074
LOC105378083 ; LOC107986664 ; TAGAP
0.790 0.320 6 159044945 5 prime UTR variant T/C snv 0.49 9
rs17388568
ADAD1
0.827 0.280 4 122408207 intron variant G/A snv 0.20 6
rs1794282 0.807 0.320 6 32698749 intergenic variant C/T snv 6.4E-02 6