Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12720458
KCNQ1
0.716 0.240 11 2585264 missense variant A/G snv 4.0E-05 1.4E-05 20
rs1805123
KCNH2
0.724 0.280 7 150948446 missense variant T/A;C;G snv 1.3E-05; 0.18; 8.4E-06 18
rs1805127
KCNE1
0.732 0.240 21 34449523 missense variant T/C snv 0.64 2.0E-04 17
rs767910122
KCNH2
0.724 0.280 7 150948446 frameshift variant -/GTCCG ins 4.4E-05 17
rs794728448
KCNH2
0.724 0.280 7 150948445 frameshift variant CT/G delins 17
rs41261344
SCN5A
0.763 0.120 3 38575385 missense variant C/T snv 5.4E-03 2.2E-03 11
rs1805128
KCNE1
0.776 0.160 21 34449382 missense variant C/T snv 9.4E-03 10
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
rs72546668
SSUH2 ; CAV3
0.807 0.200 3 8745644 missense variant C/A;T snv 4.0E-06; 2.6E-03 8
rs120074193
KCNQ1
0.807 0.120 11 2572870 missense variant G/A;C snv 4.0E-06 7
rs12720459
KCNQ1
0.807 0.160 11 2583535 missense variant C/A;G;T snv 7
rs17215500
KCNQ1
0.807 0.240 11 2768881 stop gained C/G;T snv 1.0E-04 7
rs199472709
KCNQ1
0.790 0.120 11 2572021 missense variant G/A;T snv 7
rs116840778
SSUH2 ; CAV3
0.882 0.200 3 8733956 missense variant G/A;C snv 7
rs786205745
CACNA1C
0.807 0.320 12 2504538 missense variant G/A;C snv 6
rs79891110
CACNA1C
0.807 0.320 12 2504944 stop gained G/A;T snv 6
rs267607277
CALM1
0.807 0.120 14 90404386 missense variant A/G snv 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
rs121912504
KCNH2
0.851 0.200 7 150951711 missense variant G/A snv 6
rs199472795
KCNQ1
0.807 0.120 11 2775984 missense variant C/T snv 7.0E-06 6
rs397508097
KCNQ1
0.807 0.120 11 2768917 stop gained C/T snv 2.8E-05 1.4E-05 6
rs137854600
SCN5A
0.807 0.120 3 38551504 missense variant C/A;T snv 6