Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913628
MYH7
0.763 0.160 14 23424059 missense variant C/G;T snv 10
rs3218713
MYH7
0.763 0.160 14 23431468 missense variant C/A;T snv 10
rs104894369
MYL2
0.807 0.080 12 110914287 missense variant C/A;T snv 10
rs113994099
POLG
0.827 0.240 15 89320883 missense variant T/C snv 10
rs121918079
TTR
0.790 0.280 18 31595143 missense variant T/C snv 10
rs121918097
TTR
0.790 0.280 18 31595137 missense variant G/A snv 10
rs193922680
ACTC1 ; LOC101928174
0.790 0.080 15 34793398 missense variant C/T snv 4.0E-06 7.0E-06 9
rs397516955
DSP
0.790 0.120 6 7562753 stop gained G/A snv 9
rs111033560
PLN ; CEP85L
0.807 0.040 6 118559037 stop gained T/G snv 1.6E-05 9
rs121912683
SLC25A4
0.851 0.200 4 185145020 missense variant C/A snv 4.0E-06 7.0E-06 9
rs11541796
TTR
0.807 0.280 18 31593011 missense variant A/G snv 9
rs1799821
CPT2
0.827 0.200 1 53210776 missense variant G/A snv 0.49 0.46 8
rs201217593
DMD
0.790 0.200 X 31177947 stop gained C/T snv 2.2E-05 2.9E-05 8
rs35049558
MYL2
0.851 0.040 12 110914287 frameshift variant -/CT ins 8.0E-06 8
rs104894724
TNNI3
0.790 0.120 19 55154146 missense variant G/A;C snv 4.0E-06 8
rs397516354
TNNI3
0.790 0.120 19 55154094 missense variant C/A;G;T snv 4.0E-05 8
rs121964856
TNNT2
0.807 0.120 1 201365297 missense variant C/A;T snv 8
rs121918090
TTR
0.790 0.240 18 31593026 missense variant G/C snv 8
rs1057517686
ATAD3A
0.827 0.120 1 1529299 missense variant C/T snv 7
rs121913002
DES
0.851 0.160 2 219425727 missense variant C/A;G;T snv 6.5E-05; 5.6E-04 7
rs74315511
NCAPH2 ; SCO2
0.925 0.240 22 50523994 missense variant C/T snv 8.0E-05 1.1E-04 7
rs1057518422
TAB2
0.851 0.240 6 149378954 stop gained C/T snv 7
rs45586240
TNNT2
0.827 0.080 1 201361989 missense variant G/A;T snv 4.0E-06 7
rs1555661648
AQP4 ; AQP4-AS1
0.882 0.240 18 26862297 missense variant C/G snv 6
rs1056892
CBR3-AS1 ; CBR3
0.882 0.160 21 36146408 missense variant G/A snv 0.37 0.39 6