Source: UNIPROT

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 1
rs36211715
MYH7
0.851 0.080 14 23424839 missense variant C/A;G;T snv 4.0E-06 1
rs371898076
MYH7
0.763 0.160 14 23426833 missense variant C/T snv 8.0E-06 4.9E-05 1
rs376897125
MYH7
0.882 0.080 14 23430601 missense variant C/T snv 1.6E-05 2.1E-05 1
rs397516088
MYH7
0.882 0.080 14 23429850 missense variant C/G;T snv 1
rs397516098
MYH7
0.882 0.080 14 23429044 missense variant C/T snv 1
rs397516101
MYH7
0.882 0.080 14 23429004 missense variant C/A;G;T snv 1
rs397516127
MYH7
0.763 0.160 14 23426834 missense variant G/A;C snv 1
rs397516157
MYH7
0.882 0.080 14 23424893 missense variant A/C;G;T snv 4.0E-06 1
rs397516161
MYH7
0.882 0.080 14 23424148 missense variant T/A;C snv 4.0E-06 1
rs397516171
MYH7
0.763 0.160 14 23424041 missense variant C/G;T snv 1
rs397516209
MYH7
0.882 0.080 14 23432713 missense variant C/T snv 4.0E-06 7.0E-06 1
rs397516260
MYH7
0.882 0.080 14 23431789 missense variant C/A;T snv 1.6E-05 1
rs397516269
MYH7
0.882 0.080 14 23431426 missense variant A/G snv 4.0E-06 1
rs727503252
MYH7
0.882 0.080 14 23424047 missense variant C/T snv 1
rs727503260
MYH7
0.851 0.080 14 23425403 missense variant C/G;T snv 1
rs727503261
MYH7
0.882 0.080 14 23425774 missense variant A/G;T snv 1
rs727503263
MYH7
0.882 0.080 14 23426810 missense variant G/A snv 1
rs727503278
MYH7
0.882 0.080 14 23432714 missense variant G/A;C;T snv 2.8E-05 1
rs727504236
MYH7
0.882 0.080 14 23428642 missense variant T/C snv 1
rs727504238
MYH7
0.882 0.080 14 23427746 missense variant T/C snv 1.6E-05 2.1E-05 1
rs727504240
MYH7
0.925 0.080 14 23426046 missense variant G/A snv 2.0E-05 1.4E-05 1
rs727504273
MYH7
0.925 0.080 14 23431781 missense variant T/G snv 7.0E-06 1
rs730880750
MYH7
0.851 0.080 14 23424843 missense variant G/A;C;T snv 1
rs730880759
MYH7
0.925 0.080 14 23424068 stop gained C/A;T snv 4.0E-06 1