Disease: Diabetes Mellitus, Insulin-Dependent
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800796
IL6-AS1 ; STEAP1B ; IL6
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
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
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs1980493
BTNL2 ; TSBP1-AS1
0.776 0.400 6 32395438 intron variant T/C snv 0.13 10
rs2027856 0.925 0.200 6 32434928 upstream gene variant G/A snv 0.18 2
rs204990
GPSM3
0.851 0.280 6 32193653 intron variant C/A;T snv 4
rs204991
GPSM3
0.882 0.200 6 32193589 intron variant T/C snv 0.21 3
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 13
rs2050189
TSBP1 ; TSBP1-AS1
0.925 0.200 6 32371870 5 prime UTR variant T/C;G snv 0.18 2
rs206015
NOTCH4
0.925 0.200 6 32214982 intron variant G/A snv 0.15 2
rs2064478
COL11A2P1
0.925 0.200 6 33104489 intron variant C/T snv 0.28 2
rs2071540
TAP1 ; PSMB9 ; PSMB8-AS1 ; PSMB8
0.925 0.200 6 32845139 non coding transcript exon variant T/C snv 0.61 2
rs2104286
IL2RA
0.662 0.440 10 6057082 intron variant T/C snv 0.18 25
rs2156875
HLA-B
0.882 0.200 6 31349570 intron variant C/T snv 0.50 6
rs2187668
LOC107986589 ; HLA-DQA2 ; HLA-DQA1
0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 20
rs2239800
HLA-DQA2
0.882 0.280 6 32745490 intron variant A/G snv 0.11 3
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs2244839
HCP5 ; HCG26
0.882 0.200 6 31470591 non coding transcript exon variant G/A;T snv 3
rs2251396
MICA-AS1
0.827 0.240 6 31396930 upstream gene variant G/A snv 0.24 5
rs2253907 0.882 0.360 6 31369093 intron variant C/T snv 0.43 3
rs2254556 0.851 0.280 6 31374854 intron variant T/C snv 0.85 4
rs2260000
PRRC2A
0.851 0.200 6 31625699 intron variant A/G snv 0.29 7
rs2267644
NOTCH4
0.925 0.200 6 32224783 upstream gene variant G/A snv 4.9E-02 2