Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7578326
LOC646736
0.882 0.080 2 226155937 TF binding site variant A/G snv 0.36 7
rs3818361
CR1
0.851 0.080 1 207611623 intron variant A/G snv 0.74 6
rs12779790 0.882 0.120 10 12286011 intergenic variant A/G snv 0.17 5
rs1036483919
GCK
0.925 0.080 7 44151050 missense variant A/G snv 4.0E-06 4
rs10770125
INS-IGF2 ; IGF2 ; IGF2-AS
0.882 0.200 11 2147784 missense variant A/G snv 0.49 0.40 4
rs193922331
LOC105375258 ; GCK
0.882 0.080 7 44147726 missense variant A/G snv 7.0E-06 4
rs1051295
KCNB1 ; LOC105372649
0.925 0.080 20 49372368 3 prime UTR variant A/G snv 0.22 3
rs7178572
HMG20A
0.925 0.120 15 77454848 intron variant A/G snv 0.63 3
rs1366600
INSR
1.000 0.080 19 7112870 3 prime UTR variant A/G snv 5.9E-02 2
rs2021966
ENPP1
1.000 0.080 6 131829299 intron variant A/G snv 0.42 2
rs2466293
LOC105375716 ; SLC30A8
1.000 0.080 8 117173699 3 prime UTR variant A/G snv 0.33 2
rs6935599
CDKAL1
1.000 0.080 6 20716864 intron variant A/G snv 0.31 2
rs7041847
GLIS3
1.000 0.080 9 4287466 intron variant A/G snv 0.37 2
rs9505118
SSR1
1.000 0.080 6 7290204 intron variant A/G snv 0.37 2
rs1042842
MFN2
1 12011623 3 prime UTR variant A/G snv 0.71 1
rs3741845
TAS2R9
12 10809516 missense variant A/G snv 0.60 0.51 1
rs7094463
TCF7L2
10 112952224 intron variant A/G snv 0.57 1
rs1800624
PBX2 ; AGER
0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 22
rs7756992
CDKAL1
0.827 0.240 6 20679478 intron variant A/G;T snv 12
rs10887800
LOC101929727 ; RNLS
0.790 0.280 10 88316086 intron variant A/G;T snv 11
rs2383208 0.882 0.120 9 22132077 downstream gene variant A/G;T snv 0.18 5
rs824248
LINGO2
0.925 0.120 9 28772702 intergenic variant A/T snv 0.23 3
rs2328549
CDKAL1
6 20718009 intron variant A/T snv 0.18 1
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56