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: rs193922401
rs193922401
ABCC8
1 1.000 0.120 11 17395914 missense variant C/A;T snv 0.710 1.000 1 2007 2007
dbSNP: rs80356611
rs80356611
KCNJ11
10 0.790 0.240 11 17387943 missense variant C/A;G;T snv 4.0E-06 0.710 1.000 1 2006 2006
dbSNP: rs141322087
rs141322087
ABCC8
13 0.851 0.160 11 17404552 missense variant C/T snv 1.2E-05 2.1E-05 0.700 0
dbSNP: rs193922396
rs193922396
ABCC8
1 1.000 0.120 11 17442744 missense variant A/G snv 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
dbSNP: rs193922399
rs193922399
ABCC8
1 1.000 0.120 11 17404527 missense variant A/C snv 0.700 0
dbSNP: rs193922400
rs193922400
ABCC8
2 0.925 0.120 11 17404524 missense variant C/A;T snv 4.0E-06 0.700 0
dbSNP: rs193922403
rs193922403
ABCC8
1 1.000 0.120 11 17395215 missense variant G/A;C snv 1.9E-04 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: rs80356624
rs80356624
KCNJ11
16 0.752 0.240 11 17387490 missense variant C/A;T snv 0.030 1.000 3 2006 2009
dbSNP: rs1285524167
rs1285524167
ABCC8
8 0.807 0.280 11 17475004 missense variant C/T snv 8.0E-06 0.020 1.000 2 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: rs137852673
rs137852673
ABCC8
4 0.851 0.120 11 17395915 missense variant G/A;T snv 5.0E-06; 2.0E-05 0.010 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: rs534808921
rs534808921
KCNJ11
1 1.000 0.120 11 17387967 missense variant C/A snv 1.2E-05 0.010 1.000 1 2020 2020
dbSNP: rs59852838
rs59852838
ABCC8
3 0.882 0.120 11 17453228 missense variant T/C snv 4.0E-05 4.9E-05 0.010 1.000 1 2008 2008