Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs74315445
KCNE1
0.807 0.120 21 34449409 missense variant C/T snv 6.8E-05 5.3E-05 2
rs120074190
KCNQ1
0.882 0.120 11 2778009 missense variant G/A snv 4.8E-05 5.6E-05 2
rs120074196
KCNQ1
0.882 0.120 11 2572057 missense variant G/A;C snv 4.0E-06 2
rs199472746
KCNQ1
0.925 0.120 11 2583445 missense variant C/T snv 4.0E-06 2
rs199472755
KCNQ1
0.851 0.120 11 2583478 missense variant C/A;G;T snv 4.0E-06 2
rs74315446
KCNE1
0.851 0.120 21 34449414 missense variant G/A;C snv 1.6E-05 1
rs199472897
KCNH2
0.925 0.120 7 150952702 missense variant T/C;G snv 1
rs28928905
KCNH2
0.851 0.120 7 150952514 missense variant C/G;T snv 1
rs104894252
KCNQ1
1.000 0.120 11 2570715 missense variant G/A;C snv 1
rs104894255
KCNQ1
1.000 0.120 11 2583459 missense variant G/A;C;T snv 1
rs120074177
KCNQ1
0.925 0.120 11 2570682 missense variant G/A;C snv 4.0E-06 1
rs120074178
KCNQ1
0.925 0.120 11 2570719 missense variant G/A;C;T snv 4.0E-06; 4.0E-06; 1.6E-05 1
rs120074179
KCNQ1
0.925 0.120 11 2572089 missense variant G/A;C;T snv 1
rs120074180
KCNQ1
1.000 0.120 11 2572882 missense variant C/G;T snv 4.0E-06 1
rs120074181
KCNQ1
0.925 0.120 11 2572981 missense variant G/A;C snv 1
rs120074182
KCNQ1
1.000 0.120 11 2583448 missense variant C/T snv 1
rs120074183
KCNQ1
1.000 0.120 11 2585213 missense variant G/A snv 1.4E-05 1
rs120074184
KCNQ1
0.925 0.120 11 2583453 missense variant G/A;C;T snv 1
rs120074185
KCNQ1
0.925 0.120 11 2776032 missense variant C/A;T snv 1.1E-05; 1.1E-05 1
rs120074186
KCNQ1
0.851 0.120 11 2572979 stop gained G/A;C;T snv 1.6E-05; 4.0E-06; 4.0E-06 1
rs120074187
KCNQ1
0.882 0.120 11 2572963 missense variant G/A snv 4.8E-05 2.1E-05 1
rs120074188
KCNQ1
0.925 0.120 11 2768902 missense variant G/A snv 4.0E-06 1
rs120074189
KCNQ1
0.851 0.120 11 2778003 missense variant C/T snv 1
rs120074191
KCNQ1
0.925 0.120 11 2445448 missense variant C/T snv 1
rs120074193
KCNQ1
0.807 0.120 11 2572870 missense variant G/A;C snv 4.0E-06 1