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: rs1805123
rs1805123
KCNH2
18 0.724 0.280 7 150948446 missense variant T/A;C;G snv 1.3E-05; 0.18; 8.4E-06 0.020 1.000 2 2011 2017
dbSNP: rs199472730
rs199472730
KCNQ1
5 0.882 0.120 11 2572895 missense variant C/G;T snv 0.020 1.000 2 2011 2018
dbSNP: rs794728448
rs794728448
KCNH2
17 0.724 0.280 7 150948445 frameshift variant CT/G delins 0.020 1.000 2 2011 2017
dbSNP: rs104894585
rs104894585
KCNJ2
5 0.851 0.120 17 70175263 missense variant C/G;T snv 0.010 1.000 1 2007 2007
dbSNP: rs11551437
rs11551437
CALM2
3 1.000 0.080 2 47161833 missense variant G/A snv 0.010 1.000 1 2016 2016
dbSNP: rs120074179
rs120074179
KCNQ1
3 0.925 0.120 11 2572089 missense variant G/A;C;T snv 0.010 1.000 1 2018 2018
dbSNP: rs120074193
rs120074193
KCNQ1
7 0.807 0.120 11 2572870 missense variant G/A;C snv 4.0E-06 0.010 < 0.001 1 2006 2006
dbSNP: rs121912504
rs121912504
KCNH2
6 0.851 0.200 7 150951711 missense variant G/A snv 0.010 1.000 1 2016 2016
dbSNP: rs1254179611
rs1254179611
KCNH2
3 1.000 0.120 7 150958295 missense variant G/A snv 0.010 1.000 1 2002 2002
dbSNP: rs143149582
rs143149582
KCNQ1
1 11 2588801 missense variant C/A snv 4.0E-06 0.010 1.000 1 2010 2010
dbSNP: rs1554919471
rs1554919471
KCNQ1
4 0.925 0.200 11 2768861 frameshift variant G/- delins 0.700 1.000 1 2018 2018
dbSNP: rs1554920808
rs1554920808
KCNQ1
3 1.000 0.120 11 2776991 missense variant A/G snv 0.700 1.000 1 2018 2018
dbSNP: rs199472718
rs199472718
KCNQ1
2 1.000 0.120 11 2572102 missense variant A/C;G snv 0.010 1.000 1 2013 2013
dbSNP: rs199472756
rs199472756
KCNQ1
3 0.925 0.120 11 2583486 missense variant G/A snv 0.010 1.000 1 2012 2012
dbSNP: rs199472823
rs199472823
KCNQ1
5 0.851 0.240 11 2571328 missense variant T/C snv 0.010 1.000 1 2011 2011
dbSNP: rs199473103
rs199473103
SCN5A
3 0.925 0.120 3 38606102 missense variant A/G snv 0.010 1.000 1 2008 2008
dbSNP: rs199473401
rs199473401
KCNQ1
4 0.925 0.120 11 2570722 missense variant T/C snv 0.010 1.000 1 2002 2002
dbSNP: rs199473470
rs199473470
KCNQ1
2 1.000 0.120 11 2583472 missense variant C/A snv 0.010 1.000 1 2010 2010
dbSNP: rs199473605
rs199473605
SCN5A
7 0.851 0.120 3 38560374 missense variant C/G;T snv 4.8E-05; 4.0E-06 0.010 1.000 1 2009 2009
dbSNP: rs267606782
rs267606782
EMD
4 0.925 0.120 X 154379485 start lost A/G snv 0.010 1.000 1 2015 2015
dbSNP: rs554903493
rs554903493
SLCO6A1
2 1.000 0.120 5 102419940 missense variant G/A snv 8.2E-06 0.010 1.000 1 2008 2008
dbSNP: rs566251672
rs566251672
SCN5A
2 1.000 0.120 3 38587437 missense variant C/A;T snv 4.0E-06; 1.6E-05 0.010 1.000 1 2013 2013
dbSNP: rs587777907
rs587777907
KCNH2
2 1.000 0.120 7 150958319 missense variant T/A snv 2.0E-05 0.010 1.000 1 2015 2015
dbSNP: rs762510312
rs762510312
KCNH2
3 0.925 0.120 7 150946956 missense variant G/A;C snv 4.8E-05; 1.2E-05 0.010 1.000 1 2012 2012
dbSNP: rs7626962
rs7626962
SCN5A
10 0.790 0.080 3 38579416 missense variant G/A;T snv 1.6E-05; 5.9E-03 0.010 1.000 1 2002 2002