Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104893714
SSUH2 ; CAV3
0.925 0.120 3 8745701 missense variant T/G snv 3
rs104893907
NKX2-5
1.000 5 173232776 stop gained A/C;T snv 3
rs104894021
KCNH2
0.851 0.120 7 150951629 missense variant G/C;T snv 5
rs104894228
LRRC56 ; HRAS
0.605 0.560 11 534286 missense variant C/A;G;T snv 48
rs104894230
HRAS ; LRRC56
0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs104894503
TPM1
0.776 0.160 15 63060899 missense variant G/A snv 1.6E-05 2.8E-05 9
rs104894584
KCNJ2
0.851 0.120 17 70175553 missense variant G/A snv 5
rs1057128
KCNQ1
11 2776007 synonymous variant G/A snv 0.21 0.16 1
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs120074192
KCNQ1
0.763 0.120 11 2527959 missense variant A/G snv 10
rs120074195
KCNQ1
0.925 0.120 11 2572984 missense variant G/A;C snv 3
rs1204372364
ANK2
1.000 0.120 4 113355900 missense variant T/C snv 8.0E-06 7.0E-06 2
rs121912507
KCNH2
0.882 0.120 7 150951511 missense variant C/G;T snv 4
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
rs1249958
PPP1R1A
0.925 0.040 12 54582053 missense variant C/T snv 2.7E-02 3
rs1254113735
PKP2
12 32822599 missense variant G/C snv 1
rs1254179611
KCNH2
1.000 0.120 7 150958295 missense variant G/A snv 3
rs1316189390
HCN4 ; LOC105370890
1.000 0.040 15 73343594 missense variant T/C snv 4.0E-06 2
rs1339374391
LMNA
1 156135973 synonymous variant C/T snv 4.0E-06 1
rs1355262401
GJA1
1.000 0.080 6 121447691 missense variant T/G snv 7.0E-06 2
rs1370940194
KCNA5
12 5044419 missense variant C/T snv 4.4E-06 1
rs137854602
SCN5A
0.925 0.080 3 38555664 missense variant G/A snv 5.6E-05 1.4E-05 5
rs137854605
SCN5A
1.000 0.120 3 38581337 missense variant GA/TT mnv 2
rs137854606
SCN5A
0.882 0.120 3 38604062 missense variant C/A snv 4