Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs121434386
SCN4B
0.925 0.120 11 118141265 missense variant G/A snv 7.0E-06 2
rs121434500
SNTA1
0.851 0.120 20 33410203 missense variant G/A snv 2.0E-05 1.4E-05 5
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
rs12720458
KCNQ1
0.716 0.240 11 2585264 missense variant A/G snv 4.0E-05 1.4E-05 20
rs12720459
KCNQ1
0.807 0.160 11 2583535 missense variant C/A;G;T snv 7
rs137854601
SCN5A
0.776 0.120 3 38551022 stop gained C/A;T snv 4.0E-06 10
rs1480085793
SCN5A
1.000 0.120 3 38620919 stop gained G/A snv 4.0E-06 1
rs151344631
KCNQ1
0.827 0.200 11 2571333 missense variant G/A snv 8.0E-06 3.5E-05 5
rs16847548 0.807 0.120 1 162065484 upstream gene variant T/C snv 0.22 8
rs1805123
KCNH2
0.724 0.280 7 150948446 missense variant T/A;C;G snv 1.3E-05; 0.18; 8.4E-06 18
rs1805127
KCNE1
0.732 0.240 21 34449523 missense variant T/C snv 0.64 2.0E-04 17
rs1805128
KCNE1
0.776 0.160 21 34449382 missense variant C/T snv 9.4E-03 10
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
rs199472815
KCNQ1
0.851 0.120 11 2778024 missense variant G/A;C snv 2.0E-05 4
rs199472910
KCNH2
0.827 0.120 7 150952508 missense variant G/A snv 1.2E-05 5
rs199472936
KCNH2
0.882 0.120 7 150951592 missense variant C/A;T snv 5
rs199472944
KCNH2
0.882 0.120 7 150951552 missense variant G/A snv 3
rs199472960
KCNH2
1.000 0.120 7 150951496 missense variant T/C snv 1
rs199472990
KCNH2
0.882 0.120 7 150950312 missense variant G/A snv 7.0E-06 3
rs199473051
SCN5A
0.925 0.120 3 38633058 missense variant C/T snv 2
rs199473103
SCN5A
0.925 0.120 3 38606102 missense variant A/G snv 3
rs199473225
SCN5A
0.851 0.120 3 38560397 missense variant G/A;C snv 6
rs199473317
SCN5A
0.882 0.120 3 38551003 missense variant T/C snv 3