Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397508087
KCNQ1
1.000 0.120 11 2588799 frameshift variant C/-;CC delins 2
rs137854606
SCN5A
0.882 0.120 3 38604062 missense variant C/A snv 4
rs184442491
SCN5A
1.000 0.120 3 38603888 missense variant C/A snv 2.1E-04 7.7E-04 2
rs35530544
ANK2
1.000 0.080 4 113367751 missense variant C/A snv 2.5E-03 1.0E-02 2
rs104894230
HRAS ; LRRC56
0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs104894228
LRRC56 ; HRAS
0.605 0.560 11 534286 missense variant C/A;G;T snv 48
rs199473283
SCN5A
1.000 0.120 3 38551495 missense variant C/A;G;T snv 4.0E-05 2
rs137854618
SCN5A
0.742 0.120 3 38566426 missense variant C/A;T snv 8.0E-06 15
rs80338777
CACNA1S
0.827 0.200 1 201077915 missense variant C/A;T snv 1.2E-05 10
rs199472936
KCNH2
0.882 0.120 7 150951592 missense variant C/A;T snv 5
rs779640835
RYR2
1.000 0.040 1 237566723 missense variant C/A;T snv 4.0E-06; 2.8E-05 2
rs121918606
RYR2
0.925 0.080 1 237819181 missense variant C/G snv 3
rs370819854
SCN5A
3 38551456 missense variant C/G snv 8.0E-06 1
rs199473605
SCN5A
0.851 0.120 3 38560374 missense variant C/G;T snv 4.8E-05; 4.0E-06 7
rs121912507
KCNH2
0.882 0.120 7 150951511 missense variant C/G;T snv 4
rs58327533
LMNA
1.000 0.120 1 156114991 missense variant C/G;T snv 4
rs5443
CDCA3 ; GNB3
0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs2200733 0.752 0.240 4 110789013 intergenic variant C/T snv 0.18 12
rs60682848
LMNA
0.790 0.200 1 156134838 stop gained C/T snv 7.0E-06 11
rs1805128
KCNE1
0.776 0.160 21 34449382 missense variant C/T snv 9.4E-03 10
rs199473648
LOC105372791 ; KCNE2
1.000 0.080 21 34370507 missense variant C/T snv 2.5E-04 2.4E-04 4
rs1249958
PPP1R1A
0.925 0.040 12 54582053 missense variant C/T snv 2.7E-02 3
rs199473631
SCN5A
0.925 0.120 3 38551085 missense variant C/T snv 3
rs45627438
SCN5A
0.925 0.080 3 38604025 missense variant C/T snv 5.8E-05 2.8E-05 3
rs199472762
KCNQ1
1.000 0.120 11 2583540 missense variant C/T snv 2