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
rs12720458
KCNQ1
0.716 0.240 11 2585264 missense variant A/G snv 4.0E-05 1.4E-05 20
rs267607277
CALM1
0.807 0.120 14 90404386 missense variant A/G snv 6
rs199473103
SCN5A
0.925 0.120 3 38606102 missense variant A/G snv 3
rs4657139 0.925 0.120 1 162060117 intergenic variant A/T snv 0.48 3
rs199473447
KCNQ1
1.000 0.120 11 2445412 missense variant A/T snv 1
rs12720459
KCNQ1
0.807 0.160 11 2583535 missense variant C/A;G;T snv 7
rs199473428
KCNH2
0.851 0.120 7 150951643 missense variant C/A;G;T snv 8.0E-06 4
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
rs794728879
SCN5A
0.925 0.120 3 38560146 splice donor variant C/A;G;T snv 2
rs137854601
SCN5A
0.776 0.120 3 38551022 stop gained C/A;T snv 4.0E-06 10
rs199472936
KCNH2
0.882 0.120 7 150951592 missense variant C/A;T snv 5
rs199473411
KCNQ1
0.882 0.120 11 2585275 missense variant C/A;T snv 3
rs770088052
SCN5A
1.000 0.120 3 38581182 missense variant C/A;T snv 4.2E-06; 8.4E-06 1
rs780405533
SCN5A
1.000 0.120 3 38560221 stop gained C/A;T snv 3.6E-05 2.1E-05 1
rs398124650
CALM2
0.882 0.120 2 47161744 missense variant C/G;T snv 3
rs1805128
KCNE1
0.776 0.160 21 34449382 missense variant C/T snv 9.4E-03 10
rs74315445
KCNE1
0.807 0.120 21 34449409 missense variant C/T snv 6.8E-05 5.3E-05 6
rs199472696
KCNQ1
0.851 0.120 11 2570670 missense variant C/T snv 4.0E-06 1.4E-05 4
rs199472719
KCNQ1
0.882 0.120 11 2572104 missense variant C/T snv 4.1E-06 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
rs199473631
SCN5A
0.925 0.120 3 38551085 missense variant C/T snv 3
rs199473051
SCN5A
0.925 0.120 3 38633058 missense variant C/T snv 2
rs397508091
KCNQ1 ; KCNQ1OT1
0.925 0.120 11 2662080 stop gained C/T snv 2