Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121918462
PTPN11
0.742 0.320 12 112450398 missense variant C/T snv 13
rs397507549
PTPN11
0.742 0.240 12 112489104 missense variant C/A;G snv 13
rs104894201
CRYAB
0.763 0.280 11 111908934 missense variant T/C snv 12
rs104894369
MYL2
0.807 0.080 12 110914287 missense variant C/A;T snv 10
rs104894231
LRRC56 ; HRAS
0.776 0.360 11 533467 missense variant C/G;T snv 9
rs121964856
TNNT2
0.807 0.120 1 201365297 missense variant C/A;T snv 8
rs1057517686
ATAD3A
0.827 0.120 1 1529299 missense variant C/T snv 7
rs104894502
TPM1
0.807 0.120 15 63060915 missense variant A/G;T snv 6
rs1057519819
MAP2K1
0.851 0.240 15 66436750 missense variant T/C snv 6
rs116840805
SSUH2 ; CAV3
0.827 0.160 3 8745725 missense variant C/T snv 6
rs121908991
PRKAG2
0.807 0.120 7 151560610 missense variant C/A;T snv 6
rs121964858
TNNT2
0.807 0.120 1 201365244 missense variant A/C;G;T snv 6
rs104894729
TNNI3
0.827 0.080 19 55151892 missense variant C/A;G;T snv 5
rs104894204
CSRP3
0.882 0.040 11 19188245 missense variant A/C snv 4
rs104894630
SCO1
0.882 0.120 17 10692805 missense variant G/A snv 4
rs1157637439
VARS2
0.882 0.120 6 30920187 missense variant A/G snv 4
rs121913624
MYH7
0.851 0.080 14 23429278 missense variant C/A;G;T snv 4
rs121913625
MYH7
0.851 0.080 14 23429005 missense variant G/A;C;T snv 4
rs121917758
LRRC56 ; HRAS
0.851 0.160 11 533883 missense variant G/A snv 4
rs199476314
TPM1
0.882 0.040 15 63060930 missense variant T/G snv 4
rs267607158
TTN ; TTN-AS1
0.851 0.040 2 178740125 stop gained G/A snv 4
rs397514616
TNNC1
0.851 0.120 3 52452217 missense variant C/A;T snv 4
rs1057517105
GAA
0.882 0.160 17 80112655 missense variant G/A snv 3
rs121913634
MYH7
0.882 0.080 14 23425372 missense variant T/A;C snv 3
rs121913652
MYH7 ; MHRT
0.882 0.080 14 23414015 missense variant C/T snv 7.0E-06 3