Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs199473442
KCNQ1
1.000 0.120 11 2445103 missense variant C/G;T snv 3
rs762510312
KCNH2
0.925 0.120 7 150946956 missense variant G/A;C snv 4.8E-05; 1.2E-05 3
rs786205753
CACNA1C
0.925 0.080 12 2593255 missense variant G/A snv 3
rs915012109
SMYD1
0.925 0.040 2 88096710 missense variant T/C snv 4.0E-06 7.0E-06 3
rs1047624774
ATP2B4
1.000 0.120 1 203700807 missense variant T/C snv 4.0E-06 3.5E-05 2
rs1287693879
DNAH8
1.000 0.120 6 38737083 missense variant T/C snv 7.0E-06 2
rs139467962
SNTA1
1.000 0.120 20 33412702 missense variant G/A snv 1.6E-05 4.9E-05 2
rs199472718
KCNQ1
1.000 0.120 11 2572102 missense variant A/C;G snv 2
rs199473012
KCNH2
1.000 0.120 7 150947708 missense variant G/C snv 2.6E-05 4.2E-05 2
rs199473470
KCNQ1
1.000 0.120 11 2583472 missense variant C/A snv 2
rs554903493
SLCO6A1
1.000 0.120 5 102419940 missense variant G/A snv 8.2E-06 2
rs566251672
SCN5A
1.000 0.120 3 38587437 missense variant C/A;T snv 4.0E-06; 1.6E-05 2
rs587777907
KCNH2
1.000 0.120 7 150958319 missense variant T/A snv 2.0E-05 2
rs143149582
KCNQ1
11 2588801 missense variant C/A snv 4.0E-06 1
rs5751876
ADORA2A ; ADORA2A-AS1 ; SPECC1L-ADORA2A
0.742 0.320 22 24441333 synonymous variant T/C snv 0.54 0.52 16
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
rs1554919471
KCNQ1
0.925 0.200 11 2768861 frameshift variant G/- delins 4
rs267606782
EMD
0.925 0.120 X 154379485 start lost A/G snv 4
rs878854378
TTN ; TTN-AS1
0.742 0.320 2 178533657 inframe deletion GTT/- delins 33