Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs120074192
KCNQ1
0.763 0.120 11 2527959 missense variant A/G snv 10
rs16847548 0.807 0.120 1 162065484 upstream gene variant T/C snv 0.22 8
rs116840778
SSUH2 ; CAV3
0.882 0.200 3 8733956 missense variant G/A;C snv 7
rs12720459
KCNQ1
0.807 0.160 11 2583535 missense variant C/A;G;T snv 7
rs199472709
KCNQ1
0.790 0.120 11 2572021 missense variant G/A;T snv 7
rs121912504
KCNH2
0.851 0.200 7 150951711 missense variant G/A snv 6
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
rs398124647
CALM2
0.807 0.120 2 47161851 missense variant T/A;C snv 6
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
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
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
rs28928905
KCNH2
0.851 0.120 7 150952514 missense variant C/G;T snv 5
rs587782933
CACNA1C
0.827 0.200 12 2504526 missense variant G/A snv 5
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
rs137854615
SCN5A
0.851 0.120 3 38550989 missense variant A/G snv 4
rs199473401
KCNQ1
0.925 0.120 11 2570722 missense variant T/C snv 4
rs199473604
SCN5A
0.882 0.120 3 38560394 missense variant G/T snv 4