Disease: elevated blood glucose level
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs2971672
GCK
7 44166307 intron variant A/C snv 0.44 4
rs4253252
KLKB1
4 186236304 intron variant T/G snv 0.56 3
rs4329
ACE
17 63486097 intron variant A/C;G snv 2
rs4581570 13 27936575 intergenic variant T/A;C snv 2
rs477992
PHGDH
1 119714953 intron variant A/G snv 0.69 4
rs494562 6 85407411 intergenic variant A/G snv 0.16 2
rs503279
FUT2 ; LOC105447645
19 48705753 3 prime UTR variant T/C snv 0.48 2
rs57884925
GLIS3
9 4285119 intron variant C/G;T snv 2
rs60808706
KCNQ1
11 2836003 intron variant G/A snv 0.12 4
rs612169
ABO
9 133268030 intron variant G/A snv 10
rs61824877
LINC00862
1 200273504 intron variant G/A snv 0.11 3
rs6499165
SLC7A6OS ; SLC7A6
16 68292297 non coding transcript exon variant A/C snv 0.80 2
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
rs6975024
GCK
7 44192287 intron variant T/C snv 0.14 4
rs7200543
PDXDC1
16 15036113 synonymous variant A/G snv 0.35 0.30 6
rs76185967
RPL35P6 ; PSD3
8 18774816 non coding transcript exon variant C/T snv 1.6E-02 2
rs7760535
REV3L ; MFSD4B
6 111425880 intron variant G/C snv 0.46 3
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 24
rs8396
ETFDH ; PPID
4 158709665 3 prime UTR variant T/C snv 0.29 4
rs9332998
CYP4A11
1 46938514 intron variant T/C snv 0.16 2
rs9393903
ELOVL2 ; ELOVL2-AS1
6 11042676 intron variant G/A snv 0.18 3
rs9942416 5 75741470 intergenic variant C/G snv 0.53 9