Disease: elevated blood glucose level
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10799701 1 21494497 intergenic variant A/G snv 0.47 2
rs12753193 1 65703996 non coding transcript exon variant G/A snv 0.58 3
rs211718
SLC44A5
1 75640990 downstream gene variant T/C snv 0.75 3
rs2794520 0.807 0.240 1 159709026 upstream gene variant C/A;T snv 9
rs477992
PHGDH
1 119714953 intron variant A/G snv 0.69 4
rs61824877
LINC00862
1 200273504 intron variant G/A snv 0.11 3
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 22
rs9332998
CYP4A11
1 46938514 intron variant T/C snv 0.16 2
rs9943291
HMGCS2
1 119749667 intron variant T/G snv 8.2E-02 3
rs12053049
SPC25
2 168910638 intron variant T/C snv 5.2E-02 2
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs12712928 2 44964941 intron variant G/C snv 0.18 2
rs13391552
ALMS1
2 73591809 intron variant G/A;C snv 2
rs1349497
RAPGEF4-AS1
2 172727935 intron variant G/A;C snv 2
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 19
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
rs2232326
SPC25 ; G6PC2
2 168907981 missense variant T/C snv 5.1E-03 3.3E-03 3
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 18
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 18
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 21
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
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs887829
UGT1A8 ; UGT1A5 ; UGT1A6 ; UGT1A7 ; UGT1A4 ; UGT1A3 ; UGT1A10 ; UGT1A1 ; UGT1A9
0.763 0.280 2 233759924 intron variant C/T snv 0.36 18