Disease: Diabetes Mellitus, Insulin-Dependent
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1001179
CAT
0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 33
rs10181656
STAT4
0.763 0.360 2 191105153 intron variant G/C snv 0.79 9
rs10735810
VDR
0.662 0.640 12 47879112 start lost A/C;G;T snv 26
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs10758593
GLIS3
0.827 0.240 9 4292083 intron variant G/A snv 0.45 8
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs11154178
LOC105377982 ; TRDN
0.807 0.240 6 123540174 intron variant T/A;C snv 7
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 18
rs1131580
TNFSF10
0.882 0.160 3 172505830 3 prime UTR variant A/C;G;T snv 4
rs11568820
VDR
0.672 0.480 12 47908762 intron variant C/T snv 0.38 27
rs12255372
TCF7L2
0.667 0.480 10 113049143 intron variant G/A;T snv 28
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv 25
rs1332629192
ALB
0.851 0.200 4 73404374 missense variant C/T snv 7
rs1358030 0.925 0.120 10 106363841 intergenic variant G/A snv 0.57 2
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs1555212014
HNF1A
0.807 0.280 12 120994264 missense variant C/T snv 6
rs17300539
ADIPOQ
0.752 0.320 3 186841671 upstream gene variant G/A snv 5.3E-02 11
rs1800624
PBX2 ; AGER
0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs1800783
NOS3
0.827 0.280 7 150992309 intron variant A/C;G;T snv 7
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
rs2107538
LOC105371744 ; CCL5
0.763 0.360 17 35880776 5 prime UTR variant C/T snv 0.27 11
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61