Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10224002
PRKAG2
0.925 0.080 7 151717955 intron variant A/G snv 0.31 12
rs2278426
ANGPTL8 ; DOCK6
1.000 0.080 19 11239812 missense variant C/T snv 0.11 0.11 11
rs1128249
COBLL1
1.000 0.080 2 164672114 intron variant G/C;T snv 10
rs2925979
CMIP
1.000 0.080 16 81501185 intron variant T/A;C snv 10
rs649129 1.000 0.080 9 133278860 upstream gene variant T/C;G snv 10
rs11708067
ADCY5
0.882 0.080 3 123346931 intron variant A/G snv 0.19 9
rs13389219
COBLL1
1.000 0.080 2 164672366 intron variant C/T snv 0.47 9
rs137853240
HNF1A
0.807 0.080 12 120994405 missense variant G/A snv 1.4E-05 8
rs17482753 1.000 0.080 8 19975135 regulatory region variant G/T snv 8.8E-02 8
rs4607517
GCK
0.882 0.080 7 44196069 intron variant G/A;C snv 8
rs7607980
COBLL1
1.000 0.080 2 164694691 missense variant T/C snv 0.11 0.13 8
rs9368222
CDKAL1
1.000 0.080 6 20686765 intron variant C/A;T snv 8
rs10195252
COBLL1
0.925 0.080 2 164656581 intron variant T/C snv 0.48 7
rs2000999
HPR ; TXNL4B
1.000 0.080 16 72074194 intron variant G/A snv 0.16 7
rs340874
PROX1 ; PROX1-AS1
0.882 0.080 1 213985913 non coding transcript exon variant T/C snv 0.40 7
rs679899
APOB
0.925 0.080 2 21028042 missense variant G/A snv 0.49 0.39 7
rs7578326
LOC646736
0.882 0.080 2 226155937 TF binding site variant A/G snv 0.36 7
rs900400
LINC02029
0.925 0.080 3 157080986 upstream gene variant T/C snv 0.36 7
rs11048456
LOC105369705
1.000 0.080 12 26310149 intron variant C/T snv 0.62 6
rs1799884
GCK
1.000 0.080 7 44189469 intron variant C/T snv 0.17 6
rs1800574
HNF1A ; HNF1A-AS1
0.882 0.080 12 120979061 missense variant C/T snv 2.9E-02 2.2E-02 6
rs757110
ABCC8
0.851 0.080 11 17396930 missense variant C/A;T snv 0.64; 8.0E-06 6
rs76895963
CCND2-AS1 ; CCND2
1.000 0.080 12 4275678 intron variant T/G snv 1.5E-02 6
rs80356610
KCNJ11
0.827 0.080 11 17387968 missense variant A/G snv 6
rs10184004 1.000 0.080 2 164651879 downstream gene variant C/T snv 0.48 5