Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121908987
PRKAG2
0.742 0.200 7 151576412 missense variant C/A;G;T snv 4.0E-06 12
rs60682848
LMNA
0.790 0.200 1 156134838 stop gained C/T snv 7.0E-06 11
rs120074192
KCNQ1
0.763 0.120 11 2527959 missense variant A/G snv 10
rs3825214
TBX5
0.851 0.080 12 114357638 intron variant G/A snv 0.77 8
rs121913003
DES
0.882 0.200 2 219421532 missense variant C/T snv 6
rs267598596
KCNQ4
0.827 0.120 1 40818164 missense variant G/A snv 5
rs57629361
LMNA
0.827 0.280 1 156137207 missense variant C/A;G;T snv 9.3E-06 5
rs41310765
SCN5A
0.882 0.120 3 38575424 missense variant G/A snv 1.4E-04 7.7E-05 5
rs199473039
KCNH2
0.851 0.120 7 150951512 missense variant G/A;C;T snv 9.5E-05 4
rs120074189
KCNQ1
0.851 0.120 11 2778003 missense variant C/T snv 4
rs72549410
SCN5A
0.851 0.120 3 38606058 missense variant C/T snv 4
rs199472954
KCNH2
0.882 0.120 7 150951514 missense variant A/G;T snv 3
rs104894074
GATA4
0.925 0.120 8 11708467 missense variant C/T snv 2
rs759067821
GATA4
1.000 0.080 8 11758294 missense variant C/T snv 2.8E-05 1.4E-05 2
rs758277832
NKX2-5
1.000 0.080 5 173233109 missense variant G/C snv 2
rs172149856
TRPM4
0.925 0.080 19 49188641 missense variant G/A snv 5.1E-04 4.3E-04 2
rs753734843
HCN4
1.000 0.080 15 73322804 missense variant C/A;T snv 6.6E-06; 2.6E-05 1