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: rs193929358
rs193929358
KCNJ11
5 0.851 0.240 11 17387091 missense variant C/T snv 0.010 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 0.010 1.000 1 2017 2017
dbSNP: rs80356615
rs80356615
KCNJ11
4 0.851 0.240 11 17387934 missense variant C/T snv 0.010 1.000 1 2008 2008
dbSNP: rs80356616
rs80356616
KCNJ11
19 0.732 0.360 11 17387917 missense variant C/T snv 0.010 1.000 1 2011 2011
dbSNP: rs80356637
rs80356637
ABCC8
4 0.851 0.240 11 17470119 missense variant A/C;G snv 0.010 1.000 1 2006 2006