Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057517686
ATAD3A
0.827 0.120 1 1529299 missense variant C/T snv 7
rs121909374
MYBPC3
0.790 0.120 11 47342578 stop gained C/A;G snv 1.3E-05 7
rs121913630
MYH7
0.851 0.080 14 23425814 missense variant G/A;C snv 1.2E-05 7
rs150821281
PKP2
0.827 0.080 12 32878461 missense variant G/A snv 2.3E-03 2.5E-03 7
rs45586240
TNNT2
0.827 0.080 1 201361989 missense variant G/A;T snv 4.0E-06 7
rs587782951
JPH2
0.807 0.080 20 44160305 missense variant G/T snv 6
rs1057519819
MAP2K1
0.851 0.240 15 66436750 missense variant T/C snv 6
rs371401403
MYBPC3
0.807 0.080 11 47335996 missense variant G/A;T snv 6.8E-05; 7.9E-05 6
rs267606910
MYH7
0.807 0.080 14 23431589 missense variant C/T snv 8.0E-06 6
rs863224900
MYH7
0.807 0.160 14 23428534 missense variant A/C;G;T snv 6
rs121908991
PRKAG2
0.807 0.120 7 151560610 missense variant C/A;T snv 6
rs116840805
SSUH2 ; CAV3
0.827 0.160 3 8745725 missense variant C/T snv 6
rs267607124
TNNC1
0.807 0.080 3 52451410 missense variant G/A;C;T snv 4.0E-05; 4.0E-06; 1.3E-04 6
rs397516349
TNNI3
0.807 0.080 19 55154145 missense variant C/T snv 1.6E-05 6
rs727503504
TNNI3
0.807 0.080 19 55154071 missense variant G/A;C snv 6
rs121964858
TNNT2
0.807 0.120 1 201365244 missense variant A/C;G;T snv 6
rs74315379
TNNT2
0.827 0.080 1 201364336 missense variant G/A;T snv 1.2E-04 6
rs104894502
TPM1
0.807 0.120 15 63060915 missense variant A/G;T snv 6
rs199476301
TPM1
0.851 0.040 15 63042874 missense variant G/A;T snv 4.0E-06 6
rs1057518933
CASR
0.851 0.160 3 122284403 missense variant G/A snv 5
rs56657623
LMNA
0.827 0.120 1 156138540 missense variant G/A snv 1.6E-05 7.0E-06 5
rs61444459
LMNA
0.851 0.160 1 156137667 missense variant G/A;C snv 5
rs36211723
MYBPC3
0.851 0.080 11 47338520 missense variant C/G;T snv 1.6E-05 5
rs375882485
MYBPC3
0.827 0.080 11 47342698 missense variant G/A snv 4.0E-05 9.8E-05 5
rs397515905
MYBPC3
0.851 0.080 11 47342719 missense variant G/A;C;T snv 4.0E-06; 8.0E-06 5