Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs863224900
MYH7
0.807 0.160 14 23428534 missense variant A/C;G;T snv 6
rs104893823
TNNC1
0.882 0.040 3 52451285 missense variant C/T snv 5
rs104894729
TNNI3
0.827 0.080 19 55151892 missense variant C/A;G;T snv 5
rs1057518933
CASR
0.851 0.160 3 122284403 missense variant G/A snv 5
rs1566535410
MYH7
0.851 0.080 14 23429297 missense variant T/C snv 5
rs199476315
TPM1
0.827 0.080 15 63061723 missense variant G/A snv 5
rs397516347
TNNI3
0.851 0.120 19 55154157 missense variant C/T snv 4.2E-05 5
rs397516357
TNNI3
0.851 0.120 19 55151910 missense variant C/T snv 7.0E-06 5
rs606231324
MYH7
0.851 0.080 14 23428505 missense variant C/G;T snv 5
rs61444459
LMNA
0.851 0.160 1 156137667 missense variant G/A;C snv 5
rs727503166
MYBPC3
0.851 0.080 11 47332110 frameshift variant T/- del 5
rs727503204
MYBPC3
0.882 0.080 11 47343020 splice donor variant C/G;T snv 5
rs727503503
TNNI3
0.827 0.120 19 55154070 missense variant C/T snv 5
rs727504246
TNNT2
0.827 0.080 1 201363330 missense variant G/A 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
rs121913638
MYH7
0.851 0.120 14 23425980 missense variant 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
rs267607125
TNNC1 ; NISCH
0.851 0.080 3 52453993 missense variant G/A snv 7.0E-06 4
rs267607158
TTN ; TTN-AS1
0.851 0.040 2 178740125 stop gained G/A snv 4
rs28933098
MYH7 ; MHRT
0.882 0.160 14 23415021 missense variant G/A;T snv 4