Disease: Diabetes
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1004446
IGF2 ; INS-IGF2 ; IGF2-AS
0.827 0.240 11 2148913 intron variant G/A snv 0.37 7
rs10517086
LINC02357
0.882 0.160 4 26083889 intron variant G/A snv 0.27 4
rs11203203
UBASH3A
0.807 0.240 21 42416077 intron variant G/A snv 0.28 9
rs12255372
TCF7L2
0.667 0.480 10 113049143 intron variant G/A;T snv 28
rs1233478
LINC02829
0.925 0.120 6 29510044 intron variant G/A;C;T snv 3
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv 25
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
rs187238
IL18
0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs2290400
GSDMB
0.790 0.360 17 39909987 intron variant T/C snv 0.48 9
rs4402960
IGF2BP2
0.724 0.400 3 185793899 intron variant G/T snv 0.38 21
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 22
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 18
rs6476839
GLIS3
0.925 0.120 9 4290823 intron variant A/C;T snv 3
rs7533564
MGC27382 ; PTGFR
0.925 0.120 1 78360228 intron variant C/T snv 0.92 4
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 10
rs4900384 0.882 0.160 14 98032614 intergenic variant A/G snv 0.40 4
rs2111485 0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46 17
rs5219
KCNJ11
0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 25
rs713041
GPX4
0.776 0.400 19 1106616 stop gained T/A;C snv 4.2E-06; 0.58 16
rs1042713
ADRB2
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63