Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs137854607
SCN5A
0.882 0.120 3 38554309 missense variant C/G;T 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
rs56793579
LMNA
0.851 0.240 1 156115102 missense variant C/G;T 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
rs786205436
SDHD
0.882 0.080 11 112088972 missense variant A/G;T snv 5
rs863225119
TNNT2
0.882 0.080 1 201359632 missense variant T/A snv 5
rs104894204
CSRP3
0.882 0.040 11 19188245 missense variant A/C snv 4
rs111033559
PLN ; CEP85L
0.925 0.040 6 118558946 missense variant C/T snv 4
rs121912557
MYO6
0.882 0.120 6 75857198 missense variant G/A snv 4
rs1553707780
TTN-AS1 ; TTN
0.925 0.040 2 178616928 frameshift variant T/- del 4
rs267606782
EMD
0.925 0.120 X 154379485 start lost A/G snv 4
rs267607004
RBM20
0.925 0.040 10 110812304 missense variant G/A snv 1.4E-05 4
rs267607571
LMNA
0.882 0.160 1 156134458 missense variant G/A;T snv 4
rs387907339
CRYAB
0.882 0.280 11 111908967 missense variant C/A;G snv 4
rs397516088
MYH7
0.882 0.080 14 23429850 missense variant C/G;T snv 4
rs397516165
MYH7
0.925 0.080 14 23424118 missense variant C/G;T snv 4
rs397516373
TPM1
0.925 0.080 15 63059663 missense variant G/A snv 4
rs397516607
RBM20
0.925 0.040 10 110821356 missense variant G/A snv 4
rs397516706
DSG2-AS1 ; DSG2
0.925 0.080 18 31546441 frameshift variant AGAG/-;AG delins 4
rs397516784
CEP85L ; PLN
0.925 0.080 6 118558957 inframe deletion AGA/- delins 1.4E-05 4
rs45544633
MHRT ; MYH7
1.000 0.080 14 23417174 missense variant G/A snv 4
rs56816490
LMNA
0.925 0.120 1 156135913 stop gained G/A;T snv 4
rs63750743
TMEM43
0.925 0.080 3 14141665 missense variant C/T snv 4