Disease: Glucose measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1495743 8 18415790 intergenic variant G/A;C snv 6
rs2624265
LINC02694
15 38856448 intron variant T/C snv 0.28 3
rs2971672
GCK
7 44166307 intron variant A/C snv 0.44 4
rs7200543
PDXDC1
16 15036113 synonymous variant A/G snv 0.35 0.30 6
rs9942416 5 75741470 intergenic variant C/G snv 0.53 9
rs10096633 1.000 0.040 8 19973410 regulatory region variant C/T snv 0.22 8
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
rs12420422 0.851 0.120 11 123009573 intergenic variant G/A snv 3.4E-02 16
rs12579302
ATP2B1
0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv 16
rs17140821 0.851 0.120 7 19177581 regulatory region variant G/A snv 7.9E-02 16
rs1869717
MAML3
0.851 0.120 4 139829967 intron variant G/C snv 0.14 16
rs222826 0.851 0.120 2 146120964 regulatory region variant T/C snv 0.94 16
rs261332
ALDH1A2 ; LIPC-AS1 ; LIPC
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 20
rs2866611 0.851 0.120 20 41322165 upstream gene variant A/T snv 0.58 16
rs2980853 0.851 0.120 8 125466108 upstream gene variant A/C snv 0.43 16
rs4704221
CERT1
0.851 0.120 5 75463358 intron variant T/A;C snv 16
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 18
rs4905014
ITPK1
0.851 0.120 14 92945686 intron variant G/A;C snv 16
rs5744680
POLK
0.851 0.120 5 75584065 intron variant G/A snv 0.55 18
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 22
rs6533530 0.851 0.120 4 110810780 intergenic variant T/C snv 0.47 16
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 14
rs6759518
SLC30A3
0.851 0.120 2 27263727 intron variant G/C snv 5.5E-02 16