Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057518916
SCN5A
3 38606034 stop gained G/A snv 1
rs143149582
KCNQ1
11 2588801 missense variant C/A snv 4.0E-06 1
rs868064163
ACTL6A
1.000 0.040 3 179586552 missense variant C/T snv 7.0E-06 13
rs915012109
SMYD1
0.925 0.040 2 88096710 missense variant T/C snv 4.0E-06 7.0E-06 3
rs7626962
SCN5A
0.790 0.080 3 38579416 missense variant G/A;T snv 1.6E-05; 5.9E-03 10
rs104894485
HCN4
0.882 0.080 15 73325378 missense variant C/T snv 3.6E-05 7.0E-06 4
rs11551437
CALM2
1.000 0.080 2 47161833 missense variant G/A snv 3
rs786205753
CACNA1C
0.925 0.080 12 2593255 missense variant G/A snv 3
rs120074193
KCNQ1
0.807 0.120 11 2572870 missense variant G/A;C snv 4.0E-06 7
rs199473605
SCN5A
0.851 0.120 3 38560374 missense variant C/G;T snv 4.8E-05; 4.0E-06 7
rs104894585
KCNJ2
0.851 0.120 17 70175263 missense variant C/G;T snv 5
rs121434500
SNTA1
0.851 0.120 20 33410203 missense variant G/A snv 2.0E-05 1.4E-05 5
rs199472730
KCNQ1
0.882 0.120 11 2572895 missense variant C/G;T snv 5
rs199473401
KCNQ1
0.925 0.120 11 2570722 missense variant T/C snv 4
rs267606782
EMD
0.925 0.120 X 154379485 start lost A/G snv 4
rs120074179
KCNQ1
0.925 0.120 11 2572089 missense variant G/A;C;T snv 3
rs1254179611
KCNH2
1.000 0.120 7 150958295 missense variant G/A snv 3
rs1554920808
KCNQ1
1.000 0.120 11 2776991 missense variant A/G snv 3
rs199472756
KCNQ1
0.925 0.120 11 2583486 missense variant G/A snv 3
rs199473103
SCN5A
0.925 0.120 3 38606102 missense variant A/G snv 3
rs199473442
KCNQ1
1.000 0.120 11 2445103 missense variant C/G;T snv 3
rs762510312
KCNH2
0.925 0.120 7 150946956 missense variant G/A;C snv 4.8E-05; 1.2E-05 3
rs1047624774
ATP2B4
1.000 0.120 1 203700807 missense variant T/C snv 4.0E-06 3.5E-05 2
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