Disease: elevated blood glucose level
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1558318 1.000 0.080 7 15025987 intergenic variant A/T snv 0.55 3
rs17140821 0.851 0.120 7 19177581 regulatory region variant G/A snv 7.9E-02 16
rs17168486
DGKB
1.000 0.080 7 14858657 intron variant C/T snv 0.18 5
rs17277546
TRIM4
7 99891948 3 prime UTR variant G/A snv 3.1E-02 4
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 19
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs1869717
MAML3
0.851 0.120 4 139829967 intron variant G/C snv 0.14 16
rs2023634
DGCR9 ; DGCR5
22 18984937 intron variant A/G snv 7.9E-02 2
rs2066938
UNC119B ; MIR4700
12 120722812 3 prime UTR variant A/C;G snv 3
rs2074755
BAZ1B
0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02 20
rs2087160
ENPEP
4 110413574 intron variant G/T snv 0.68 2
rs211718
SLC44A5
1 75640990 downstream gene variant T/C snv 0.75 3
rs2216405 2 210752170 intergenic variant A/G snv 0.15 2
rs222826 0.851 0.120 2 146120964 regulatory region variant T/C snv 0.94 16
rs2403254
HPS5
11 18303599 intron variant C/G;T snv 2
rs2411884
KCNQ1
11 2714304 intron variant C/A;G snv 2
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 20
rs2518049
AKR1C3
10 5095844 intron variant A/G;T snv 2
rs261332
ALDH1A2 ; LIPC-AS1 ; LIPC
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 20
rs2624265
LINC02694
15 38856448 intron variant T/C snv 0.28 3
rs2650000
HNF1A-AS1
0.851 0.200 12 120951159 intron variant A/C snv 0.70 10
rs2652822
LACTB ; RPS27L
15 63130573 3 prime UTR variant T/C snv 0.41 2
rs272889
SLC22A4 ; MIR3936HG
5 132329685 intron variant A/G snv 0.64 2
rs2794520 0.807 0.240 1 159709026 upstream gene variant C/A;T snv 9
rs2866611 0.851 0.120 20 41322165 upstream gene variant A/T snv 0.58 16