Disease: Diabetes Mellitus, Insulin-Dependent
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3733197
BANK1
0.742 0.320 4 101918130 missense variant G/A snv 0.31 0.30 13
rs2304256
TYK2
0.732 0.360 19 10364976 missense variant C/A snv 0.27 0.23 13
rs1800587
IL1A
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 26
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 22
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 18
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 20
rs907715
IL21
0.752 0.520 4 122613898 intron variant C/T snv 0.35 11
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 18
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs3804100
TLR2
0.633 0.720 4 153704257 synonymous variant T/C snv 9.0E-02 6.7E-02 36
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs11889341
STAT4
0.732 0.480 2 191079016 intron variant C/T snv 0.21 12
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1143679
ITGAM
0.732 0.520 16 31265490 missense variant G/A snv 9.7E-02 0.11 14
rs2248462 0.807 0.240 6 31479019 downstream gene variant G/A snv 0.19 10
rs2516509
MICB-DT
0.882 0.160 6 31482217 intron variant T/C snv 0.19 7
rs2516398 0.882 0.200 6 31513749 upstream gene variant G/T snv 0.70 3
rs2844494 0.925 0.160 6 31515638 upstream gene variant C/A snv 0.70 2
rs12153855
TNXB
0.776 0.320 6 32107027 intron variant T/C snv 0.11 11
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 13