Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs111033560
PLN ; CEP85L
0.807 0.040 6 118559037 stop gained T/G snv 1.6E-05 9
rs35049558
MYL2
0.851 0.040 12 110914287 frameshift variant -/CT ins 8.0E-06 8
rs199476301
TPM1
0.851 0.040 15 63042874 missense variant G/A;T snv 4.0E-06 6
rs104893823
TNNC1
0.882 0.040 3 52451285 missense variant C/T snv 5
rs104894501
TPM1
0.851 0.040 15 63044030 stop gained G/A;C;T snv 4.0E-06 5
rs121917776
VCL
0.882 0.040 10 74112086 missense variant C/T snv 9.9E-05 7.0E-06 5
rs104894204
CSRP3
0.882 0.040 11 19188245 missense variant A/C snv 4
rs139517732
TTN
0.851 0.040 2 178802273 missense variant C/T snv 4.4E-05 1.4E-05 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
rs758264780
TPM1
0.882 0.040 15 63044029 frameshift variant G/- delins 4
rs104894205
CSRP3
0.882 0.040 11 19188286 missense variant A/G snv 1.2E-05 5.6E-05 3
rs1412710023
MYBPC3
0.925 0.040 11 47343549 missense variant T/A snv 4.1E-06 3
rs143697995
MRPL44
0.882 0.040 2 223959821 missense variant T/C;G snv 5.6E-05; 2.2E-04 3
rs1467607281
OPA1
0.882 0.040 3 193645736 missense variant T/C snv 2.1E-05 3
rs199476320
TPM1
0.925 0.040 15 63064121 missense variant C/G;T snv 3
rs267607128
TNNI3
0.882 0.040 19 55157097 missense variant G/A snv 3
rs397515985
MYBPC3
0.882 0.040 11 47335886 missense variant G/T snv 1.3E-04 2.0E-04 3
rs727502886
ACTN2
0.925 0.040 1 236719007 missense variant G/A snv 3
rs727503269
MYH7
0.882 0.040 14 23429329 missense variant T/C snv 3
rs730880336
MYBPC3
0.925 0.040 11 47346254 frameshift variant -/TGCCG delins 4.0E-06 3
rs730880850
MYH7
0.882 0.040 14 23431584 splice donor variant C/T snv 4.0E-06 3
rs730881098
TNNT2
0.882 0.040 1 201365613 missense variant A/C snv 3
rs746536347
ATAD3B
0.882 0.040 1 1490639 missense variant C/T snv 2.6E-05 3.5E-05 3
rs750745310
DNM1L ; YARS2
0.882 0.040 12 32743390 missense variant C/T snv 3