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: 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: 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: 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: 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: rs193922565
rs193922565
KCNJ11
1 1.000 0.120 11 17388087 missense variant A/G snv 0.700 0
dbSNP: rs587783673
rs587783673
KCNJ11
2 1.000 0.120 11 17387407 missense variant C/T snv 0.020 1.000 2 2017 2018
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: rs758604661
rs758604661
ABCC8
2 0.925 0.120 11 17474898 missense variant A/G snv 8.0E-06 0.010 1.000 1 2014 2014
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: 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: 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: rs193922400
rs193922400
ABCC8
2 0.925 0.120 11 17404524 missense variant C/A;T snv 4.0E-06 0.700 0
dbSNP: rs193922408
rs193922408
ABCC8
2 0.925 0.120 11 17393122 missense variant C/T snv 0.700 0
dbSNP: rs193929375
rs193929375
GCK
3 0.882 0.120 7 44145560 missense variant C/A snv 0.010 1.000 1 2005 2005
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
dbSNP: rs80356663
rs80356663
INS ; INS-IGF2
3 0.925 0.120 11 2160901 missense variant G/A;T snv 0.700 0
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: 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: rs80356615
rs80356615
KCNJ11
4 0.851 0.240 11 17387934 missense variant C/T snv 0.010 1.000 1 2008 2008