Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs120074192
KCNQ1
0.763 0.120 11 2527959 missense variant A/G snv 10
rs794728708
RYR2
0.827 0.120 1 237377386 missense variant G/A;T snv 8
rs137854600
SCN5A
0.807 0.120 3 38551504 missense variant C/A;T snv 6
rs56984562
LMNA
0.827 0.200 1 156137666 missense variant C/A;G;T snv 6
rs104894584
KCNJ2
0.851 0.120 17 70175553 missense variant G/A snv 5
rs121918600
RYR2
0.882 0.080 1 237791441 missense variant C/T snv 5
rs1860561
ATP2A2
0.851 0.080 12 110345436 intron variant G/A snv 0.19 5
rs1049194905
SCN5A
0.925 0.080 3 38604063 synonymous variant A/G snv 2
rs1237080661
SCN5A
0.925 0.080 3 38604780 stop gained A/G;T snv 2.8E-05 2
rs1355262401
GJA1
1.000 0.080 6 121447691 missense variant T/G snv 7.0E-06 2
rs1554108172
DSP
0.925 0.080 6 7579983 stop gained G/T snv 2
rs104894580
KCNJ2
0.790 0.240 17 70175238 missense variant C/A;T snv 4.0E-06 7
rs199473605
SCN5A
0.851 0.120 3 38560374 missense variant C/G;T snv 4.8E-05; 4.0E-06 7
rs761056344
PLN ; CEP85L
0.925 0.080 6 118558994 missense variant C/G;T snv 4.0E-06; 3.2E-05 3
rs766265889
TTN-AS1 ; TTN
0.827 0.240 2 178535508 stop gained G/A;T snv 8.0E-06; 4.0E-06 11
rs45546039
SCN5A
0.732 0.120 3 38613781 missense variant C/A;T snv 4.1E-06 15
rs1266360671
RYR2
0.925 0.080 1 237270518 missense variant T/C snv 4.7E-06 3
rs750678689
SCN5A
0.925 0.080 3 38566466 synonymous variant G/A snv 8.0E-06 2.1E-05 2
rs764772142
RYR2
0.925 0.080 1 237377349 missense variant C/A;T snv 8.0E-06 2
rs59301204
LMNA
0.925 0.080 1 156135956 missense variant G/A;C snv 1.2E-05 4
rs104894503
TPM1
0.776 0.160 15 63060899 missense variant G/A snv 1.6E-05 2.8E-05 9
rs7626962
SCN5A
0.790 0.080 3 38579416 missense variant G/A;T snv 1.6E-05; 5.9E-03 10
rs121918604
RYR2
0.882 0.080 1 237798037 missense variant G/A;T snv 1.7E-05 3
rs765835441
RYR2
1.000 0.080 1 237726291 missense variant C/T snv 2.7E-05 2.1E-05 1
rs120074187
KCNQ1
0.882 0.120 11 2572963 missense variant G/A snv 4.8E-05 2.1E-05 3