Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs141322087
ABCC8
0.851 0.160 11 17404552 missense variant C/T snv 1.2E-05 2.1E-05 13
rs1285524167
ABCC8
0.807 0.280 11 17475004 missense variant C/T snv 8.0E-06 8
rs137852673
ABCC8
0.851 0.120 11 17395915 missense variant G/A;T snv 5.0E-06; 2.0E-05 4
rs59852838
ABCC8
0.882 0.120 11 17453228 missense variant T/C snv 4.0E-05 4.9E-05 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
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
rs193922399
ABCC8
1.000 0.120 11 17404527 missense variant A/C snv 1
rs193922401
ABCC8
1.000 0.120 11 17395914 missense variant C/A;T snv 1
rs193922403
ABCC8
1.000 0.120 11 17395215 missense variant G/A;C snv 1.9E-04 1
rs193922406
ABCC8
1.000 0.120 11 17393752 missense variant A/C snv 1
rs193922407
ABCC8
1.000 0.120 11 17393741 missense variant C/T snv 1
rs984164636
ABCC8
1.000 0.120 11 17461720 missense variant T/C snv 1
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
rs80356672
INS-IGF2 ; INS
0.925 0.120 11 2159862 missense variant T/C snv 2
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
rs80356611
KCNJ11
0.790 0.240 11 17387943 missense variant C/A;G;T snv 4.0E-06 10
rs80356618
KCNJ11
0.807 0.200 11 17387595 missense variant C/A;T snv 8