Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs886039030
MYH7
0.925 0.080 14 23426045 missense variant C/T snv 4.0E-06 2.8E-05 1
rs727504240
MYH7
0.925 0.080 14 23426046 missense variant G/A snv 2.0E-05 1.4E-05 1
rs727503263
MYH7
0.882 0.080 14 23426810 missense variant G/A snv 1
rs371898076
MYH7
0.763 0.160 14 23426833 missense variant C/T snv 8.0E-06 4.9E-05 1
rs397516127
MYH7
0.763 0.160 14 23426834 missense variant G/A;C snv 1
rs121913627
MYH7
0.851 0.080 14 23427657 missense variant C/A;G;T snv 4.0E-06 1
rs121913626
MYH7
0.882 0.080 14 23427723 missense variant C/A;G;T snv 4.0E-06 1
rs727504238
MYH7
0.882 0.080 14 23427746 missense variant T/C snv 1.6E-05 2.1E-05 1
rs121913642
MYH7
0.925 0.080 14 23427879 missense variant A/G snv 1
rs267606911
MYH7
0.882 0.080 14 23428587 missense variant C/A snv 8.0E-06 1
rs727504236
MYH7
0.882 0.080 14 23428642 missense variant T/C snv 1
rs397516101
MYH7
0.882 0.080 14 23429004 missense variant C/A;G;T snv 1
rs121913625
MYH7
0.851 0.080 14 23429005 missense variant G/A;C;T snv 1
rs397516098
MYH7
0.882 0.080 14 23429044 missense variant C/T snv 1
rs121913624
MYH7
0.851 0.080 14 23429278 missense variant C/A;G;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
rs376897125
MYH7
0.882 0.080 14 23430601 missense variant C/T snv 1.6E-05 2.1E-05 1
rs730880855
MYH7
0.925 0.080 14 23431425 missense variant T/C snv 1
rs397516269
MYH7
0.882 0.080 14 23431426 missense variant A/G snv 4.0E-06 1
rs121913633
MYH7
0.882 0.080 14 23431447 missense variant C/T snv 7.0E-06 1
rs3218713
MYH7
0.763 0.160 14 23431468 missense variant C/A;T snv 1
rs267606910
MYH7
0.807 0.080 14 23431589 missense variant C/T snv 8.0E-06 2