Disease: Diabetes Mellitus, Insulin-Dependent
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs763361
CD226
0.689 0.520 18 69864406 missense variant T/A;C snv 4.0E-06; 0.52 21
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs479536
NOTCH4
0.882 0.200 6 32225901 upstream gene variant G/A snv 5.0E-02 3
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 26
rs3804100
TLR2
0.633 0.720 4 153704257 synonymous variant T/C snv 9.0E-02 6.7E-02 36
rs12722495
IL2RA
0.851 0.200 10 6055320 intron variant T/C snv 7.0E-02 5
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 20
rs2856705 0.882 0.200 6 32703179 downstream gene variant C/T snv 0.11 3
rs1143679
ITGAM
0.732 0.520 16 31265490 missense variant G/A snv 9.7E-02 0.11 14
rs12153855
TNXB
0.776 0.320 6 32107027 intron variant T/C snv 0.11 11
rs9275312 0.807 0.280 6 32697951 intergenic variant A/G snv 0.16 6
rs2104286
IL2RA
0.662 0.440 10 6057082 intron variant T/C snv 0.18 25
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
rs2516509
MICB-DT
0.882 0.160 6 31482217 intron variant T/C snv 0.19 7
rs11889341
STAT4
0.732 0.480 2 191079016 intron variant C/T snv 0.21 12
rs9296015 0.851 0.280 6 32251212 upstream gene variant G/A snv 0.22 4
rs2304256
TYK2
0.732 0.360 19 10364976 missense variant C/A snv 0.27 0.23 13
rs3129763 0.827 0.280 6 32623148 TF binding site variant G/A snv 0.23 6
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 18
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 22
rs3117230 0.882 0.200 6 33107858 upstream gene variant A/G snv 0.28 3