Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042714
ADRB2
0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs45546039
SCN5A
0.732 0.120 3 38613781 missense variant C/A;T snv 4.1E-06 15
rs766265889
TTN-AS1 ; TTN
0.827 0.240 2 178535508 stop gained G/A;T snv 8.0E-06; 4.0E-06 11
rs120074192
KCNQ1
0.763 0.120 11 2527959 missense variant A/G snv 10
rs7626962
SCN5A
0.790 0.080 3 38579416 missense variant G/A;T snv 1.6E-05; 5.9E-03 10
rs3766871
RYR2
0.790 0.240 1 237614784 missense variant G/A;T snv 4.0E-02 9
rs794728708
RYR2
0.827 0.120 1 237377386 missense variant G/A;T snv 8
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
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
rs59301204
LMNA
0.925 0.080 1 156135956 missense variant G/A;C snv 1.2E-05 4
rs121918604
RYR2
0.882 0.080 1 237798037 missense variant G/A;T snv 1.7E-05 3
rs1266360671
RYR2
0.925 0.080 1 237270518 missense variant T/C snv 4.7E-06 3
rs755373114
ANK2
0.925 0.080 4 113341742 missense variant A/C snv 7.2E-05 3
rs761056344
PLN ; CEP85L
0.925 0.080 6 118558994 missense variant C/G;T snv 4.0E-06; 3.2E-05 3
rs1049194905
SCN5A
0.925 0.080 3 38604063 synonymous variant A/G snv 2
rs1554108172
DSP
0.925 0.080 6 7579983 stop gained G/T snv 2
rs740952
KCNH2
0.925 0.080 7 150952515 synonymous variant G/A;T snv 0.30; 7.2E-05 2
rs764772142
RYR2
0.925 0.080 1 237377349 missense variant C/A;T snv 8.0E-06 2
rs1355262401
GJA1
1.000 0.080 6 121447691 missense variant T/G snv 7.0E-06 2
rs120074187
KCNQ1
0.882 0.120 11 2572963 missense variant G/A snv 4.8E-05 2.1E-05 3
rs750678689
SCN5A
0.925 0.080 3 38566466 synonymous variant G/A snv 8.0E-06 2.1E-05 2