Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4607517
GCK
0.882 0.080 7 44196069 intron variant G/A;C snv 8
rs10758593
GLIS3
0.827 0.240 9 4292083 intron variant G/A snv 0.45 8
rs3749147
GPN1 ; CCDC121
0.882 0.120 2 27629051 missense variant G/A snv 0.23 0.20 8
rs6235
LOC101929710 ; PCSK1
0.925 0.120 5 96393194 missense variant C/G snv 0.26 0.23 8
rs6234
PCSK1 ; LOC101929710
0.851 0.160 5 96393270 missense variant G/C snv 0.27 0.24 8
rs10830962 0.851 0.160 11 92965261 upstream gene variant C/A;G;T snv 7
rs9356744
CDKAL1
0.882 0.120 6 20685255 intron variant T/C snv 0.42 7
rs10814916
GLIS3
0.851 0.200 9 4293150 intron variant A/C snv 0.57 7
rs340874
PROX1 ; PROX1-AS1
0.882 0.080 1 213985913 non coding transcript exon variant T/C snv 0.40 7
rs1799884
GCK
1.000 0.080 7 44189469 intron variant C/T snv 0.17 6
rs17265513
ZHX3
0.925 0.160 20 41203988 missense variant T/C snv 0.14 0.14 6
rs7936247 1.000 0.040 11 92956866 intergenic variant G/T snv 0.37 5
rs11603334
ARAP1
1.000 0.080 11 72721940 5 prime UTR variant G/A snv 0.12 5
rs11605924
CRY2
1.000 0.080 11 45851540 intron variant A/C snv 0.39 5
rs17168486
DGKB
1.000 0.080 7 14858657 intron variant C/T snv 0.18 5
rs2851682
FADS2
11 61848540 intron variant A/G snv 9.9E-02 5
rs11672660
GIPR ; MIR642B
19 45676926 intron variant C/T snv 0.18 0.17 5
rs1470579
IGF2BP2
0.925 0.160 3 185811292 intron variant A/C snv 0.46 5
rs7651090
IGF2BP2
0.925 0.080 3 185795604 intron variant A/G snv 0.39 5
rs11558471
LOC105375716 ; SLC30A8
1.000 0.080 8 117173494 3 prime UTR variant A/G snv 0.25 5
rs7944584
MADD
1.000 0.080 11 47314769 intron variant A/T snv 0.19 5
rs10501320
MADD ; MADD-AS1
0.925 0.120 11 47272248 5 prime UTR variant G/C snv 0.17 5
rs11920090
SLC2A2
1.000 0.040 3 170999732 intron variant T/A snv 0.20 5
rs8192675
SLC2A2
0.925 0.080 3 171007094 intron variant T/C snv 0.42 5
rs3802177
SLC30A8 ; LOC105375716
1.000 0.080 8 117172786 3 prime UTR variant G/A snv 0.24 5