Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3218716
MYH7
0.716 0.280 14 23425316 missense variant C/A;G;T snv 4.0E-06; 2.4E-05 17
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
rs267606908
MYH7
0.763 0.160 14 23424112 missense variant T/C snv 4.0E-06 7.0E-06 9
rs3218714
MYH7
0.763 0.160 14 23429279 missense variant G/A;C snv 9
rs371898076
MYH7
0.763 0.160 14 23426833 missense variant C/T snv 8.0E-06 4.9E-05 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
rs121913627
MYH7
0.851 0.080 14 23427657 missense variant C/A;G;T snv 4.0E-06 8
rs121913630
MYH7
0.851 0.080 14 23425814 missense variant G/A;C snv 1.2E-05 7
rs267606910
MYH7
0.807 0.080 14 23431589 missense variant C/T snv 8.0E-06 6
rs727504753
MYH7
0.807 0.160 14 23429345 missense variant C/T snv 6
rs863224900
MYH7
0.807 0.160 14 23428534 missense variant A/C;G;T snv 6
rs1566535410
MYH7
0.851 0.080 14 23429297 missense variant T/C snv 5
rs36211715
MYH7
0.851 0.080 14 23424839 missense variant C/A;G;T snv 4.0E-06 5
rs727503246
MIR208B ; MYH7
0.882 0.080 14 23418313 missense variant C/T snv 7.0E-06 4
rs121913624
MYH7
0.851 0.080 14 23429278 missense variant C/A;G;T snv 4
rs121913625
MYH7
0.851 0.080 14 23429005 missense variant G/A;C;T snv 4
rs121913638
MYH7
0.851 0.120 14 23425980 missense variant C/T snv 4
rs148808089
MYH7
0.882 0.080 14 23429038 missense variant G/A snv 2.0E-05 1.4E-05 4
rs2754158
MYH7
0.882 0.080 14 23424876 missense variant G/A;C;T snv 1.2E-05 4
rs397516088
MYH7
0.882 0.080 14 23429850 missense variant C/G;T snv 4
rs397516260
MYH7
0.882 0.080 14 23431789 missense variant C/A;T snv 1.6E-05 4
rs397516269
MYH7
0.882 0.080 14 23431426 missense variant A/G snv 4.0E-06 4