Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913626
MYH7
0.882 0.080 14 23427723 missense variant C/A;G;T snv 4.0E-06 1
rs121913624
MYH7
0.851 0.080 14 23429278 missense variant C/A;G;T snv 1
rs121913625
MYH7
0.851 0.080 14 23429005 missense variant G/A;C;T snv 1
rs121913628
MYH7
0.763 0.160 14 23424059 missense variant C/G;T snv 1
rs121913631
MYH7
0.882 0.080 14 23424107 missense variant G/C snv 1.4E-05 1
rs121913632
MYH7
0.882 0.080 14 23425760 missense variant C/A;G;T snv 1
rs121913633
MYH7
0.882 0.080 14 23431447 missense variant C/T snv 7.0E-06 1
rs121913637
MYH7
0.882 0.080 14 23425971 missense variant G/A snv 7.0E-06 1
rs121913638
MYH7
0.851 0.120 14 23425980 missense variant C/T snv 1
rs121913641
MYH7
0.882 0.080 14 23425970 missense variant C/G;T snv 1
rs121913642
MYH7
0.925 0.080 14 23427879 missense variant A/G snv 1
rs121913650
MHRT ; MYH7
0.925 0.080 14 23415652 missense variant G/A snv 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
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
rs397516171
MYH7
0.763 0.160 14 23424041 missense variant C/G;T snv 1
rs397516202
MYH7 ; MIR208B
0.882 0.080 14 23418244 missense variant C/A;T snv 7.0E-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