Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs220733
MAS1
1.000 0.080 6 159897771 intron variant A/C;G snv 0.99 3
rs104893907
NKX2-5
1.000 5 173232776 stop gained A/C;T snv 3
rs1249958
PPP1R1A
0.925 0.040 12 54582053 missense variant C/T snv 2.7E-02 3
rs121918602
RYR2
0.925 0.120 1 237454396 missense variant T/C snv 3
rs121918606
RYR2
0.925 0.080 1 237819181 missense variant C/G snv 3
rs794728721
RYR2
0.925 0.080 1 237445489 missense variant G/A snv 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
rs104893714
SSUH2 ; CAV3
0.925 0.120 3 8745701 missense variant T/G snv 3
rs397515458
TRDN ; TRDN-AS1
0.925 0.080 6 123503899 stop gained G/A snv 3.1E-05 5.6E-05 3
rs1204372364
ANK2
1.000 0.120 4 113355900 missense variant T/C snv 8.0E-06 7.0E-06 2
rs35530544
ANK2
1.000 0.080 4 113367751 missense variant C/A snv 2.5E-03 1.0E-02 2
rs1355262401
GJA1
1.000 0.080 6 121447691 missense variant T/G snv 7.0E-06 2
rs1316189390
HCN4 ; LOC105370890
1.000 0.040 15 73343594 missense variant T/C snv 4.0E-06 2
rs199473024
KCNH2
7 150947362 missense variant T/C snv 7.0E-06 2
rs794728425
KCNH2
1.000 0.120 7 150958220 frameshift variant -/GGCGATGGGAGCTGGCCGGG delins 2
rs794728470
KCNH2
1.000 0.120 7 150947367 frameshift variant -/TCGCCCCG delins 1.4E-05 2
rs794728508
KCNH2
1.000 0.120 7 150974864 frameshift variant A/- del 2
rs199473387
KCNJ2
1.000 0.120 17 70175952 missense variant A/C;G snv 2
rs199472762
KCNQ1
1.000 0.120 11 2583540 missense variant C/T snv 2
rs199473405
KCNQ1
1.000 0.120 11 2585249 missense variant A/G snv 2
rs397508087
KCNQ1
1.000 0.120 11 2588799 frameshift variant C/-;CC delins 2
rs79023478
OBSCN
1.000 0.040 1 228315865 missense variant G/A snv 8.4E-03 3.0E-02 2
rs199601548
PKP2
1.000 0.080 12 32896548 missense variant G/T snv 1.4E-04 4.0E-04 2
rs779640835
RYR2
1.000 0.040 1 237566723 missense variant C/A;T snv 4.0E-06; 2.8E-05 2