Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs3218716
MYH7
0.716 0.280 14 23425316 missense variant C/A;G;T snv 4.0E-06; 2.4E-05 17
rs121908987
PRKAG2
0.742 0.200 7 151576412 missense variant C/A;G;T snv 4.0E-06 12
rs104894369
MYL2
0.807 0.080 12 110914287 missense variant C/A;T snv 10
rs121913628
MYH7
0.763 0.160 14 23424059 missense variant C/G;T snv 10
rs3218713
MYH7
0.763 0.160 14 23431468 missense variant C/A;T snv 10
rs587782958
MYBPC3
0.790 0.120 11 47333552 splice region variant C/T snv 1.7E-05 10
rs3218714
MYH7
0.763 0.160 14 23429279 missense variant G/A;C snv 9
rs397516127
MYH7
0.763 0.160 14 23426834 missense variant G/A;C snv 9
rs397516171
MYH7
0.763 0.160 14 23424041 missense variant C/G;T snv 9
rs397516264
MYH7
0.763 0.160 14 23431602 missense variant C/T snv 4.0E-06 9
rs104894724
TNNI3
0.790 0.120 19 55154146 missense variant G/A;C snv 4.0E-06 8
rs104894845
GLA ; RPL36A-HNRNPH2
0.807 0.160 X 101401752 missense variant C/G;T snv 5.5E-04 8
rs121913627
MYH7
0.851 0.080 14 23427657 missense variant C/A;G;T snv 4.0E-06 8
rs397516354
TNNI3
0.790 0.120 19 55154094 missense variant C/A;G;T snv 4.0E-05 8
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
rs104894502
TPM1
0.807 0.120 15 63060915 missense variant A/G;T snv 6
rs121964858
TNNT2
0.807 0.120 1 201365244 missense variant A/C;G;T snv 6
rs199476317
TPM1
0.827 0.080 15 63062263 missense variant G/A snv 6
rs267606910
MYH7
0.807 0.080 14 23431589 missense variant C/T snv 8.0E-06 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
rs397516349
TNNI3
0.807 0.080 19 55154145 missense variant C/T snv 1.6E-05 6