Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3218716
MYH7
0.716 0.280 14 23425316 missense variant C/A;G;T snv 4.0E-06; 2.4E-05 17
rs121908987
PRKAG2
0.742 0.200 7 151576412 missense variant C/A;G;T snv 4.0E-06 12
rs199473119
SCN5A
0.790 0.120 3 38604035 missense variant G/A;T snv 8.4E-06; 4.2E-06 7
rs143978652
MYH6
0.882 0.080 14 23393437 missense variant C/A;T snv 9.3E-04; 4.0E-06 6
rs267606910
MYH7
0.807 0.080 14 23431589 missense variant C/T snv 8.0E-06 6
rs121908991
PRKAG2
0.807 0.120 7 151560610 missense variant C/A;T snv 6
rs121908990
PRKAG2
0.827 0.120 7 151560611 missense variant G/A;C snv 5
rs121909283
NODAL
0.882 0.120 10 70435399 stop gained C/A;T snv 3.1E-04 4
rs267606977
PRKAG2
0.851 0.120 7 151560613 missense variant T/C snv 4
rs111033205
SLC26A4 ; SLC26A4-AS1
0.882 0.240 7 107661726 stop gained G/C;T snv 9.3E-05; 6.2E-06 4
rs199472712
KCNQ1
0.882 0.120 11 2572053 missense variant G/A;T snv 4.0E-06 3
rs199472776
KCNQ1
0.882 0.120 11 2587630 missense variant C/G;T snv 4.0E-06; 2.0E-04 3
rs370544157
PRKAA1
0.882 0.160 5 40764612 missense variant C/T snv 8.0E-06 3
rs1554284604
TBX20
0.882 0.120 7 35204478 frameshift variant G/- delins 3
rs869312065
TTN ; TTN-AS1
1.000 0.080 2 178548943 stop gained G/A snv 4.0E-06 2
rs1555100687
ABCC9
1.000 0.080 12 21882764 splice donor variant A/G snv 1
rs1555418832
LOC101928174 ; ACTC1
1.000 0.080 15 34792499 frameshift variant -/G ins 1
rs760353963
MYH6
1.000 0.080 14 23383233 missense variant C/T snv 1.6E-05 1.4E-05 1
rs1131692281
PRKAG2
1.000 0.080 7 151675557 missense variant C/G;T snv 4.0E-06; 8.0E-06 1
rs79474211
PRKAG2
1.000 0.080 7 151781320 missense variant C/T snv 7.4E-03 2.2E-03 1
rs1289914935
TNNT2
1.000 0.080 1 201373252 start lost C/A;T snv 4.0E-06; 4.0E-06 1
rs1553624186
TTN ; TTN-AS1
1.000 0.080 2 178580475 synonymous variant G/A snv 1