Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs80356624
rs80356624
KCNJ11
16 0.752 0.240 11 17387490 missense variant C/A;T snv 0.030 1.000 3 2006 2009
dbSNP: rs193929337
rs193929337
KCNJ11
6 0.827 0.160 11 17387937 missense variant T/C snv 0.020 1.000 2 2014 2017
dbSNP: rs587783673
rs587783673
KCNJ11
2 1.000 0.120 11 17387407 missense variant C/T snv 0.020 1.000 2 2017 2018
dbSNP: rs80356616
rs80356616
KCNJ11
19 0.732 0.360 11 17387917 missense variant C/T snv 0.020 1.000 2 2006 2006
dbSNP: rs193922401
rs193922401
ABCC8
1 1.000 0.120 11 17395914 missense variant C/A;T snv 0.710 1.000 1 2007 2007
dbSNP: rs193922405
rs193922405
ABCC8
2 0.925 0.160 11 17394360 missense variant C/A;T snv 0.010 1.000 1 2011 2011
dbSNP: rs193929355
rs193929355
KCNJ11
4 0.882 0.120 11 17387128 missense variant C/T snv 0.010 1.000 1 2007 2007
dbSNP: rs193929373
rs193929373
GCK ; LOC105375258
4 0.882 0.120 7 44147723 missense variant C/T snv 0.010 1.000 1 2005 2005
dbSNP: rs193929375
rs193929375
GCK
3 0.882 0.120 7 44145560 missense variant C/A snv 0.010 1.000 1 2005 2005
dbSNP: rs797045209
rs797045209
ABCC8
2 0.925 0.120 11 17404525 missense variant G/A snv 7.0E-06 0.010 1.000 1 2009 2009
dbSNP: rs80356615
rs80356615
KCNJ11
4 0.851 0.240 11 17387934 missense variant C/T snv 0.010 1.000 1 2008 2008
dbSNP: rs80356618
rs80356618
KCNJ11
8 0.807 0.200 11 17387595 missense variant C/A;T snv 0.010 1.000 1 2006 2006
dbSNP: rs80356625
rs80356625
KCNJ11
6 0.827 0.280 11 17387491 missense variant G/A snv 0.010 1.000 1 2016 2016
dbSNP: rs80356672
rs80356672
INS ; INS-IGF2
2 0.925 0.120 11 2159862 missense variant T/C snv 0.010 1.000 1 2014 2014
dbSNP: rs984164636
rs984164636
ABCC8
1 1.000 0.120 11 17461720 missense variant T/C snv 0.010 1.000 1 2017 2017
dbSNP: rs193922396
rs193922396
ABCC8
1 1.000 0.120 11 17442744 missense variant A/G snv 0.700 0
dbSNP: rs193922399
rs193922399
ABCC8
1 1.000 0.120 11 17404527 missense variant A/C snv 0.700 0
dbSNP: rs193922406
rs193922406
ABCC8
1 1.000 0.120 11 17393752 missense variant A/C snv 0.700 0
dbSNP: rs193922407
rs193922407
ABCC8
1 1.000 0.120 11 17393741 missense variant C/T snv 0.700 0
dbSNP: rs193922408
rs193922408
ABCC8
2 0.925 0.120 11 17393122 missense variant C/T snv 0.700 0
dbSNP: rs193922565
rs193922565
KCNJ11
1 1.000 0.120 11 17388087 missense variant A/G snv 0.700 0
dbSNP: rs80356663
rs80356663
INS ; INS-IGF2
3 0.925 0.120 11 2160901 missense variant G/A;T snv 0.700 0
dbSNP: rs779736828
rs779736828
ABCC8
2 0.925 0.120 11 17413396 missense variant G/A;T snv 4.0E-06; 4.0E-06 0.010 1.000 1 2014 2014
dbSNP: rs193922400
rs193922400
ABCC8
2 0.925 0.120 11 17404524 missense variant C/A;T snv 4.0E-06 0.700 0
dbSNP: rs193922397
rs193922397
ABCC8
1 1.000 0.120 11 17442734 missense variant T/C snv 4.0E-06 0.700 0