Disease: elevated blood glucose level
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11705729
IGF2BP2
1.000 0.080 3 185789511 intron variant A/T snv 0.45 3
rs1558318 1.000 0.080 7 15025987 intergenic variant A/T snv 0.55 3
rs2866611 0.851 0.120 20 41322165 upstream gene variant A/T snv 0.58 16
rs12670403
LOC101927609 ; AHR
7 17269655 intron variant C/A snv 0.46 2
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 20
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 18
rs8082812 0.851 0.120 18 8522684 intergenic variant C/A snv 4.6E-02 16
rs2411884
KCNQ1
11 2714304 intron variant C/A;G snv 2
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv 16
rs13266634
SLC30A8 ; LOC105375716
0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 23
rs2794520 0.807 0.240 1 159709026 upstream gene variant C/A;T snv 9
rs760762
PLCG1
0.851 0.120 20 41147406 intron variant C/A;T snv 0.59 16
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 24
rs6558295
GPAA1
8 144084619 intron variant C/G snv 8.1E-02 0.14 2
rs662138
SLC22A1
6 160143444 intron variant C/G snv 0.14 2
rs9942416 5 75741470 intergenic variant C/G snv 0.53 9
rs2403254
HPS5
11 18303599 intron variant C/G;T snv 2
rs57884925
GLIS3
9 4285119 intron variant C/G;T snv 2
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs10096633 1.000 0.040 8 19973410 regulatory region variant C/T snv 0.22 8
rs10518693
IVD
15 40407823 intron variant C/T snv 0.37 2
rs12310617 0.851 0.120 12 3060327 intergenic variant C/T snv 0.11 16
rs12369179
ZCCHC8
0.851 0.120 12 122479003 intron variant C/T snv 5.9E-02 16
rs17168486
DGKB
1.000 0.080 7 14858657 intron variant C/T snv 0.18 5
rs4481233
SLC2A9
0.925 0.120 4 9954455 intron variant C/T snv 0.16 5