Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs80356616
KCNJ11
0.732 0.360 11 17387917 missense variant C/T snv 19
rs80356624
KCNJ11
0.752 0.240 11 17387490 missense variant C/A;T snv 16
rs141322087
ABCC8
0.851 0.160 11 17404552 missense variant C/T snv 1.2E-05 2.1E-05 13
rs80356611
KCNJ11
0.790 0.240 11 17387943 missense variant C/A;G;T snv 4.0E-06 10
rs1285524167
ABCC8
0.807 0.280 11 17475004 missense variant C/T snv 8.0E-06 8
rs80356618
KCNJ11
0.807 0.200 11 17387595 missense variant C/A;T snv 8
rs193929337
KCNJ11
0.827 0.160 11 17387937 missense variant T/C snv 6
rs80356625
KCNJ11
0.827 0.280 11 17387491 missense variant G/A snv 6
rs137852673
ABCC8
0.851 0.120 11 17395915 missense variant G/A;T snv 5.0E-06; 2.0E-05 4
rs193929355
KCNJ11
0.882 0.120 11 17387128 missense variant C/T snv 4
rs80356615
KCNJ11
0.851 0.240 11 17387934 missense variant C/T snv 4
rs193929373
LOC105375258 ; GCK
0.882 0.120 7 44147723 missense variant C/T snv 4
rs59852838
ABCC8
0.882 0.120 11 17453228 missense variant T/C snv 4.0E-05 4.9E-05 3
rs193929375
GCK
0.882 0.120 7 44145560 missense variant C/A snv 3
rs80356663
INS-IGF2 ; INS
0.925 0.120 11 2160901 missense variant G/A;T snv 3
rs193922400
ABCC8
0.925 0.120 11 17404524 missense variant C/A;T snv 4.0E-06 2
rs193922405
ABCC8
0.925 0.160 11 17394360 missense variant C/A;T snv 2
rs193922408
ABCC8
0.925 0.120 11 17393122 missense variant C/T snv 2
rs758604661
ABCC8
0.925 0.120 11 17474898 missense variant A/G snv 8.0E-06 2
rs779736828
ABCC8
0.925 0.120 11 17413396 missense variant G/A;T snv 4.0E-06; 4.0E-06 2
rs797045209
ABCC8
0.925 0.120 11 17404525 missense variant G/A snv 7.0E-06 2
rs80356672
INS-IGF2 ; INS
0.925 0.120 11 2159862 missense variant T/C snv 2
rs587783673
KCNJ11
1.000 0.120 11 17387407 missense variant C/T snv 2
rs193922396
ABCC8
1.000 0.120 11 17442744 missense variant A/G snv 1
rs193922397
ABCC8
1.000 0.120 11 17442734 missense variant T/C snv 4.0E-06 1