Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs193929373
LOC105375258 ; GCK
0.882 0.120 7 44147723 missense variant C/T snv 4
rs193929375
GCK
0.882 0.120 7 44145560 missense variant C/A snv 3
rs59852838
ABCC8
0.882 0.120 11 17453228 missense variant T/C snv 4.0E-05 4.9E-05 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
rs193922408
ABCC8
0.925 0.120 11 17393122 missense variant C/T snv 2
rs587783673
KCNJ11
1.000 0.120 11 17387407 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
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
rs193922565
KCNJ11
1.000 0.120 11 17388087 missense variant A/G snv 1
rs534808921
KCNJ11
1.000 0.120 11 17387967 missense variant C/A snv 1.2E-05 1
rs984164636
ABCC8
1.000 0.120 11 17461720 missense variant T/C snv 1
rs141322087
ABCC8
0.851 0.160 11 17404552 missense variant C/T snv 1.2E-05 2.1E-05 13
rs193929337
KCNJ11
0.827 0.160 11 17387937 missense variant T/C snv 6