Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397516201
MYH7 ; MIR208B
0.882 0.080 14 23418249 missense variant G/A snv 4.0E-06 1.4E-05 1
rs397516202
MYH7 ; MIR208B
0.882 0.080 14 23418244 missense variant C/A;T snv 7.0E-06 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
rs727503246
MIR208B ; MYH7
0.882 0.080 14 23418313 missense variant C/T snv 7.0E-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
rs730880855
MYH7
0.925 0.080 14 23431425 missense variant T/C snv 1
rs886039030
MYH7
0.925 0.080 14 23426045 missense variant C/T snv 4.0E-06 2.8E-05 1
rs121913638
MYH7
0.851 0.120 14 23425980 missense variant C/T snv 1
rs121913628
MYH7
0.763 0.160 14 23424059 missense variant C/G;T snv 1
rs121913647
MHRT ; MYH7
0.925 0.160 14 23417173 missense variant C/A;G;T snv 1.6E-05 1
rs267606908
MYH7
0.763 0.160 14 23424112 missense variant T/C snv 4.0E-06 7.0E-06 1
rs3218713
MYH7
0.763 0.160 14 23431468 missense variant C/A;T snv 1
rs3218714
MYH7
0.763 0.160 14 23429279 missense variant G/A;C snv 1