Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913627
MYH7
0.851 0.080 14 23427657 missense variant C/A;G;T snv 4.0E-06 8
rs121913630
MYH7
0.851 0.080 14 23425814 missense variant G/A;C snv 1.2E-05 7
rs267606910
MYH7
0.807 0.080 14 23431589 missense variant C/T snv 8.0E-06 6
rs1566535410
MYH7
0.851 0.080 14 23429297 missense variant T/C snv 5
rs36211715
MYH7
0.851 0.080 14 23424839 missense variant C/A;G;T snv 4.0E-06 5
rs121913624
MYH7
0.851 0.080 14 23429278 missense variant C/A;G;T snv 4
rs121913625
MYH7
0.851 0.080 14 23429005 missense variant G/A;C;T snv 4
rs148808089
MYH7
0.882 0.080 14 23429038 missense variant G/A snv 2.0E-05 1.4E-05 4
rs2754158
MYH7
0.882 0.080 14 23424876 missense variant G/A;C;T snv 1.2E-05 4
rs397516088
MYH7
0.882 0.080 14 23429850 missense variant C/G;T snv 4
rs397516260
MYH7
0.882 0.080 14 23431789 missense variant C/A;T snv 1.6E-05 4
rs397516269
MYH7
0.882 0.080 14 23431426 missense variant A/G snv 4.0E-06 4
rs727503246
MIR208B ; MYH7
0.882 0.080 14 23418313 missense variant C/T snv 7.0E-06 4
rs727503260
MYH7
0.851 0.080 14 23425403 missense variant C/G;T snv 4
rs730880750
MYH7
0.851 0.080 14 23424843 missense variant G/A;C;T snv 4
rs121913626
MYH7
0.882 0.080 14 23427723 missense variant C/A;G;T snv 4.0E-06 3
rs121913631
MYH7
0.882 0.080 14 23424107 missense variant G/C snv 1.4E-05 3
rs121913632
MYH7
0.882 0.080 14 23425760 missense variant C/A;G;T snv 3
rs121913633
MYH7
0.882 0.080 14 23431447 missense variant C/T snv 7.0E-06 3
rs121913634
MYH7
0.882 0.080 14 23425372 missense variant T/A;C snv 3
rs121913637
MYH7
0.882 0.080 14 23425971 missense variant G/A snv 7.0E-06 3
rs121913641
MYH7
0.882 0.080 14 23425970 missense variant C/G;T snv 3
rs121913652
MYH7 ; MHRT
0.882 0.080 14 23414015 missense variant C/T snv 7.0E-06 3
rs186964570
MYH7
0.882 0.080 14 23433656 missense variant G/A snv 5.3E-04 2.2E-04 3
rs193922390
MHRT ; MYH7
0.882 0.080 14 23415651 missense variant C/G;T snv 4.0E-06; 2.0E-05 3