Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35049558
MYL2
0.851 0.040 12 110914287 frameshift variant -/CT ins 8.0E-06 8
rs104894204
CSRP3
0.882 0.040 11 19188245 missense variant A/C snv 4
rs730881098
TNNT2
0.882 0.040 1 201365613 missense variant A/C snv 3
rs121964858
TNNT2
0.807 0.120 1 201365244 missense variant A/C;G;T snv 6
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs1157637439
VARS2
0.882 0.120 6 30920187 missense variant A/G snv 4
rs267606979
PRKAG2
0.882 0.080 7 151560560 missense variant A/G snv 3
rs397516130
MYH7
0.882 0.080 14 23426033 missense variant A/G snv 3
rs1060501436
MYH7
0.925 0.040 14 23424815 missense variant A/G snv 2
rs199476322
TPM1
0.925 0.040 15 63064141 missense variant A/G snv 7.0E-06 2
rs759589565
TXNRD1
0.925 0.040 12 104321227 missense variant A/G snv 4.0E-05 3.5E-05 2
rs779782995
HDAC9
0.925 0.040 7 18590438 missense variant A/G snv 1.7E-05 2
rs104894502
TPM1
0.807 0.120 15 63060915 missense variant A/G;T snv 6
rs267607123
TNNC1
0.882 0.080 3 52452222 missense variant A/T snv 4.0E-06 7.0E-06 4
rs76863441
PLA2G7
0.672 0.440 6 46709361 missense variant C/A snv 4.5E-03 1.3E-03 25
rs397507549
PTPN11
0.742 0.240 12 112489104 missense variant C/A;G snv 13
rs730880751
MYH7
0.925 0.040 14 23424816 missense variant C/A;G snv 2
rs121913627
MYH7
0.851 0.080 14 23427657 missense variant C/A;G;T snv 4.0E-06 8
rs104894729
TNNI3
0.827 0.080 19 55151892 missense variant C/A;G;T snv 5
rs36211715
MYH7
0.851 0.080 14 23424839 missense variant C/A;G;T snv 4.0E-06 5
rs121913624
MYH7
0.851 0.080 14 23429278 missense variant C/A;G;T snv 4
rs104894369
MYL2
0.807 0.080 12 110914287 missense variant C/A;T snv 10
rs121964856
TNNT2
0.807 0.120 1 201365297 missense variant C/A;T snv 8
rs121908991
PRKAG2
0.807 0.120 7 151560610 missense variant C/A;T snv 6
rs573916965
MYBPC3
0.827 0.080 11 47346297 stop gained C/A;T snv 2.5E-04 5