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
rs1805127
KCNE1
0.732 0.240 21 34449523 missense variant T/C snv 0.64 2.0E-04 17
rs199473457
KCNQ1
0.827 0.200 11 2572020 missense variant C/A;T snv 12
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
rs74315445
KCNE1
0.807 0.120 21 34449409 missense variant C/T snv 6.8E-05 5.3E-05 6
rs17221854
KCNQ1
0.807 0.120 11 2777990 missense variant C/T snv 1.6E-05 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
rs199472910
KCNH2
0.827 0.120 7 150952508 missense variant G/A snv 1.2E-05 5
rs28928905
KCNH2
0.851 0.120 7 150952514 missense variant C/G;T snv 5
rs143709408
KCNQ1
0.882 0.200 11 2527999 missense variant C/T snv 1.6E-04 3.6E-04 5
rs151344631
KCNQ1
0.827 0.200 11 2571333 missense variant G/A snv 8.0E-06 3.5E-05 5
rs199472730
KCNQ1
0.882 0.120 11 2572895 missense variant C/G;T snv 5
rs74315446
KCNE1
0.851 0.120 21 34449414 missense variant G/A;C snv 1.6E-05 4
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
rs120074196
KCNQ1
0.882 0.120 11 2572057 missense variant G/A;C snv 4.0E-06 4
rs199472696
KCNQ1
0.851 0.120 11 2570670 missense variant C/T snv 4.0E-06 1.4E-05 4
rs199472755
KCNQ1
0.851 0.120 11 2583478 missense variant C/A;G;T snv 4.0E-06 4
rs199472815
KCNQ1
0.851 0.120 11 2778024 missense variant G/A;C snv 2.0E-05 4
rs199473401
KCNQ1
0.925 0.120 11 2570722 missense variant T/C snv 4
rs397508118
KCNQ1
0.851 0.120 11 2570720 frameshift variant GCGCT/- delins 1.4E-05 4