Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs199472990
KCNH2
0.882 0.120 7 150950312 missense variant G/A snv 7.0E-06 3
rs199473103
SCN5A
0.925 0.120 3 38606102 missense variant A/G snv 3
rs199473317
SCN5A
0.882 0.120 3 38551003 missense variant T/C snv 3
rs199473411
KCNQ1
0.882 0.120 11 2585275 missense variant C/A;T snv 3
rs199473456
KCNQ1
0.882 0.120 11 2571394 missense variant C/T snv 1.2E-05 3
rs199473522
KCNH2
0.882 0.120 7 150951583 missense variant C/T snv 3
rs199473538
KCNH2
0.882 0.120 7 150948981 missense variant G/A snv 4.0E-06 7.0E-06 3
rs199473631
SCN5A
0.925 0.120 3 38551085 missense variant C/T snv 3
rs398124650
CALM2
0.882 0.120 2 47161744 missense variant C/G;T snv 3
rs121434386
SCN4B
0.925 0.120 11 118141265 missense variant G/A snv 7.0E-06 2
rs12720449
KCNQ1
0.925 0.120 11 2588804 missense variant C/A;G;T snv 7.2E-05; 7.5E-03; 2.0E-05 2
rs199473051
SCN5A
0.925 0.120 3 38633058 missense variant C/T snv 2
rs199473394
KCNQ1
0.925 0.120 11 2570685 missense variant G/A snv 7.0E-06 2
rs199473507
KCNH2
0.925 0.120 7 150952723 missense variant T/C snv 2
rs554903493
SLCO6A1
1.000 0.120 5 102419940 missense variant G/A snv 8.2E-06 2
rs769505732
KCNH2
0.925 0.120 7 150952696 missense variant G/A snv 4.0E-06 2
rs794728568
KCNQ1
0.925 0.120 11 2570707 missense variant G/A;T snv 2
rs199472960
KCNH2
1.000 0.120 7 150951496 missense variant T/C snv 1
rs199473359
KCNE1
1.000 0.120 21 34449393 missense variant T/A;C snv 8.0E-06 1
rs199473447
KCNQ1
1.000 0.120 11 2445412 missense variant A/T snv 1
rs770088052
SCN5A
1.000 0.120 3 38581182 missense variant C/A;T snv 4.2E-06; 8.4E-06 1
rs794728879
SCN5A
0.925 0.120 3 38560146 splice donor variant C/A;G;T snv 2
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
rs397508118
KCNQ1
0.851 0.120 11 2570720 frameshift variant GCGCT/- delins 1.4E-05 4