Disease: Diabetes Mellitus, Insulin-Dependent
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46
rs1801275
IL4R
0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 58
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805011
IL4R
0.776 0.320 16 27362551 missense variant A/C;G;T snv 0.13; 1.2E-04; 3.6E-05 8
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs187238
IL18
0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 14
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs1990760
IFIH1
0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 33
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs2187668
LOC107986589 ; HLA-DQA2 ; HLA-DQA1
0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 20
rs222747
TRPV1
0.827 0.240 17 3589906 missense variant C/A;G;T snv 0.72; 4.5E-06 8
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs2277460
PSMA6
0.882 0.200 14 35292367 5 prime UTR variant C/A;T snv 3
rs2290400
GSDMB
0.790 0.360 17 39909987 intron variant T/C snv 0.48 9
rs2295826
PSMC6
0.851 0.200 14 52708205 intron variant A/G snv 0.11 4
rs2295827
PSMC6
0.851 0.200 14 52708263 intron variant C/T snv 9.6E-02 9.1E-02 4
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 10
rs2348071
ARMH4 ; PSMA3
0.827 0.240 14 58263908 intron variant A/G snv 0.71 5
rs2395185
HLA-DRB9
0.724 0.360 6 32465390 intron variant G/T snv 0.29 17
rs2407992
TLR8 ; TLR8-AS1
0.882 0.200 X 12920993 synonymous variant G/A;C snv 0.54 4
rs241425
TAP2
0.925 0.160 6 32837132 intron variant A/C;G snv 2