Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs41261344
SCN5A
0.763 0.120 3 38575385 missense variant C/T snv 5.4E-03 2.2E-03 11
rs120074192
KCNQ1
0.763 0.120 11 2527959 missense variant A/G snv 10
rs137854601
SCN5A
0.776 0.120 3 38551022 stop gained C/A;T snv 4.0E-06 10
rs16847548 0.807 0.120 1 162065484 upstream gene variant T/C snv 0.22 8
rs120074193
KCNQ1
0.807 0.120 11 2572870 missense variant G/A;C snv 4.0E-06 7
rs199472709
KCNQ1
0.790 0.120 11 2572021 missense variant G/A;T snv 7
rs137854600
SCN5A
0.807 0.120 3 38551504 missense variant C/A;T snv 6
rs199472795
KCNQ1
0.807 0.120 11 2775984 missense variant C/T snv 7.0E-06 6
rs267607277
CALM1
0.807 0.120 14 90404386 missense variant A/G snv 6
rs397508097
KCNQ1
0.807 0.120 11 2768917 stop gained C/T snv 2.8E-05 1.4E-05 6
rs398124647
CALM2
0.807 0.120 2 47161851 missense variant T/A;C snv 6
rs74315445
KCNE1
0.807 0.120 21 34449409 missense variant C/T snv 6.8E-05 5.3E-05 6
rs121434500
SNTA1
0.851 0.120 20 33410203 missense variant G/A snv 2.0E-05 1.4E-05 5
rs12720452
SCN5A
0.882 0.120 3 38603758 missense variant C/T snv 2.9E-04 2.9E-04 5
rs199472687
KCNQ1
0.827 0.120 11 2527962 missense variant G/A snv 5
rs199472730
KCNQ1
0.882 0.120 11 2572895 missense variant C/G;T snv 5
rs199472910
KCNH2
0.827 0.120 7 150952508 missense variant G/A snv 1.2E-05 5
rs199472921
KCNH2
0.882 0.120 7 150951712 missense variant C/G;T snv 5
rs199472936
KCNH2
0.882 0.120 7 150951592 missense variant C/A;T snv 5
rs199473282
SCN5A
0.827 0.120 3 38551513 missense variant G/A;T snv 4.0E-06 5
rs28928905
KCNH2
0.851 0.120 7 150952514 missense variant C/G;T snv 5
rs397516042
MYBPC3
0.827 0.120 11 47332075 stop gained G/A snv 8.1E-06 7.0E-06 5
rs120074186
KCNQ1
0.851 0.120 11 2572979 stop gained G/A;C;T snv 1.6E-05; 4.0E-06; 4.0E-06 4
rs120074189
KCNQ1
0.851 0.120 11 2778003 missense variant C/T snv 4
rs121912507
KCNH2
0.882 0.120 7 150951511 missense variant C/G;T snv 4