Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1047624774
ATP2B4
1.000 0.120 1 203700807 missense variant T/C snv 4.0E-06 3.5E-05 2
rs104894485
HCN4
0.882 0.080 15 73325378 missense variant C/T snv 3.6E-05 7.0E-06 4
rs104894585
KCNJ2
0.851 0.120 17 70175263 missense variant C/G;T snv 5
rs1057518916
SCN5A
3 38606034 stop gained G/A snv 1
rs11551437
CALM2
1.000 0.080 2 47161833 missense variant G/A snv 3
rs1178187217
DNAH11
0.683 0.480 7 21600085 missense variant G/A;T snv 4.3E-06 38
rs120074179
KCNQ1
0.925 0.120 11 2572089 missense variant G/A;C;T snv 3
rs120074193
KCNQ1
0.807 0.120 11 2572870 missense variant G/A;C snv 4.0E-06 7
rs121434500
SNTA1
0.851 0.120 20 33410203 missense variant G/A snv 2.0E-05 1.4E-05 5
rs121912504
KCNH2
0.851 0.200 7 150951711 missense variant G/A snv 6
rs1247665387
FA2H
0.807 0.360 16 74774623 missense variant C/A snv 7.0E-06 14
rs1254179611
KCNH2
1.000 0.120 7 150958295 missense variant G/A snv 3
rs1287693879
DNAH8
1.000 0.120 6 38737083 missense variant T/C snv 7.0E-06 2
rs139467962
SNTA1
1.000 0.120 20 33412702 missense variant G/A snv 1.6E-05 4.9E-05 2
rs143149582
KCNQ1
11 2588801 missense variant C/A snv 4.0E-06 1
rs1554430943
KCNH2
0.925 0.160 7 150974821 missense variant C/T snv 4
rs1554919471
KCNQ1
0.925 0.200 11 2768861 frameshift variant G/- delins 4
rs1554920808
KCNQ1
1.000 0.120 11 2776991 missense variant A/G snv 3
rs1805123
KCNH2
0.724 0.280 7 150948446 missense variant T/A;C;G snv 1.3E-05; 0.18; 8.4E-06 18
rs199472718
KCNQ1
1.000 0.120 11 2572102 missense variant A/C;G snv 2
rs199472730
KCNQ1
0.882 0.120 11 2572895 missense variant C/G;T snv 5
rs199472756
KCNQ1
0.925 0.120 11 2583486 missense variant G/A snv 3
rs199472823
KCNQ1
0.851 0.240 11 2571328 missense variant T/C snv 5
rs199473012
KCNH2
1.000 0.120 7 150947708 missense variant G/C snv 2.6E-05 4.2E-05 2
rs199473103
SCN5A
0.925 0.120 3 38606102 missense variant A/G snv 3