Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs574660186
TTN ; TTN-AS1
0.807 0.200 2 178579702 stop gained G/A;C snv 1.6E-05 3.5E-05 7
rs58596362
LMNA
0.827 0.280 1 156138613 splice region variant C/A;T snv 8.1E-06 7
rs59026483
LMNA
0.827 0.160 1 156134457 missense variant C/T snv 7.0E-06 7
rs199476301
TPM1
0.851 0.040 15 63042874 missense variant G/A;T snv 4.0E-06 6
rs199476317
TPM1
0.827 0.080 15 63062263 missense variant G/A snv 6
rs267607490
DES
0.925 0.160 2 219425734 missense variant C/T snv 6
rs397516089
MYH7
0.827 0.080 14 23429807 missense variant C/G;T snv 6
rs397516248
MYH7 ; MHRT
0.851 0.200 14 23415153 missense variant C/T snv 6
rs56984562
LMNA
0.827 0.200 1 156137666 missense variant C/A;G;T snv 6
rs57045855
LMNA
0.882 0.040 1 156134464 missense variant A/G;T snv 6
rs59270054
LMNA
0.925 0.120 1 156115162 missense variant G/A;C snv 6
rs61195471
LMNA
0.827 0.160 1 156134496 missense variant G/A snv 6
rs74315379
TNNT2
0.827 0.080 1 201364336 missense variant G/A;T snv 1.2E-04 6
rs760187215
MYH7
1.000 0.040 14 23431859 missense variant C/T snv 8.0E-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
rs201754030
TSFM
0.925 0.200 12 57796461 stop gained C/T snv 1.5E-03 1.3E-03 5
rs28933093
LMNA
0.882 0.160 1 156130741 missense variant G/A snv 5
rs397517689
TTN-AS1 ; TTN
0.882 0.160 2 178574530 stop gained G/A snv 4.0E-06 5
rs41310765
SCN5A
0.882 0.120 3 38575424 missense variant G/A snv 1.4E-04 7.7E-05 5
rs4947296 0.851 0.440 6 31090401 intergenic variant T/A;C snv 5
rs535039125
CYP2B6
0.851 0.040 19 41004380 missense variant C/T snv 1.1E-04 1.3E-04 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