Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs267606910
MYH7
0.807 0.080 14 23431589 missense variant C/T snv 8.0E-06 2
rs121913647
MHRT ; MYH7
0.925 0.160 14 23417173 missense variant C/A;G;T snv 1.6E-05 1
rs121913650
MHRT ; MYH7
0.925 0.080 14 23415652 missense variant G/A snv 7.0E-06 1
rs727503246
MIR208B ; MYH7
0.882 0.080 14 23418313 missense variant C/T snv 7.0E-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
rs121913626
MYH7
0.882 0.080 14 23427723 missense variant C/A;G;T snv 4.0E-06 1
rs121913627
MYH7
0.851 0.080 14 23427657 missense variant C/A;G;T snv 4.0E-06 1
rs121913628
MYH7
0.763 0.160 14 23424059 missense variant C/G;T snv 1
rs121913630
MYH7
0.851 0.080 14 23425814 missense variant G/A;C snv 1.2E-05 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
rs202141173
MYH7
0.882 0.080 14 23424842 missense variant C/T snv 2.4E-05 9.1E-05 1
rs2069544
MYH7
0.882 0.080 14 23425371 missense variant G/A;C;T snv 2.9E-04 1
rs267606908
MYH7
0.763 0.160 14 23424112 missense variant T/C snv 4.0E-06 7.0E-06 1
rs267606911
MYH7
0.882 0.080 14 23428587 missense variant C/A snv 8.0E-06 1
rs2754158
MYH7
0.882 0.080 14 23424876 missense variant G/A;C;T snv 1.2E-05 1
rs2856897
MYH7
0.925 0.080 14 23424875 missense variant C/A;G;T snv 4.0E-06; 1.2E-05 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