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: rs1047624774
rs1047624774
ATP2B4
2 1.000 0.120 1 203700807 missense variant T/C snv 4.0E-06 3.5E-05 0.010 1.000 1 2013 2013
dbSNP: rs104894485
rs104894485
HCN4
4 0.882 0.080 15 73325378 missense variant C/T snv 3.6E-05 7.0E-06 0.010 1.000 1 2004 2004
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: rs1057518916
rs1057518916
SCN5A
1 3 38606034 stop gained G/A snv 0.700 0
dbSNP: rs11551437
rs11551437
CALM2
3 1.000 0.080 2 47161833 missense variant G/A snv 0.010 1.000 1 2016 2016
dbSNP: rs1178187217
rs1178187217
DNAH11
38 0.683 0.480 7 21600085 missense variant G/A;T snv 4.3E-06 0.700 0
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: rs121434500
rs121434500
SNTA1
5 0.851 0.120 20 33410203 missense variant G/A snv 2.0E-05 1.4E-05 0.010 1.000 1 2008 2008
dbSNP: rs121912504
rs121912504
KCNH2
6 0.851 0.200 7 150951711 missense variant G/A snv 0.010 1.000 1 2016 2016
dbSNP: rs1247665387
rs1247665387
FA2H
14 0.807 0.360 16 74774623 missense variant C/A snv 7.0E-06 0.700 0
dbSNP: rs1254179611
rs1254179611
KCNH2
3 1.000 0.120 7 150958295 missense variant G/A snv 0.010 1.000 1 2002 2002
dbSNP: rs1287693879
rs1287693879
DNAH8
2 1.000 0.120 6 38737083 missense variant T/C snv 7.0E-06 0.010 1.000 1 2013 2013
dbSNP: rs139467962
rs139467962
SNTA1
2 1.000 0.120 20 33412702 missense variant G/A snv 1.6E-05 4.9E-05 0.010 1.000 1 2013 2013
dbSNP: rs143149582
rs143149582
KCNQ1
1 11 2588801 missense variant C/A snv 4.0E-06 0.010 1.000 1 2010 2010
dbSNP: rs1554430943
rs1554430943
KCNH2
4 0.925 0.160 7 150974821 missense variant C/T snv 0.700 0
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: 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: rs199472718
rs199472718
KCNQ1
2 1.000 0.120 11 2572102 missense variant A/C;G snv 0.010 1.000 1 2013 2013
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: 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: rs199473012
rs199473012
KCNH2
2 1.000 0.120 7 150947708 missense variant G/C snv 2.6E-05 4.2E-05 0.010 1.000 1 2008 2008
dbSNP: rs199473103
rs199473103
SCN5A
3 0.925 0.120 3 38606102 missense variant A/G snv 0.010 1.000 1 2008 2008