Disease: Left ventricular noncompaction
Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs386134243
LMNA
0.708 0.360 1 156135967 missense variant C/A;T snv 4.0E-06 16
rs114638163
MIPEP
0.827 0.240 13 23805994 stop gained C/A;T snv 4.0E-06; 1.3E-03 10
rs606231324
MYH7
0.851 0.080 14 23428505 missense variant C/G;T snv 5
rs397516089
MYH7
0.827 0.080 14 23429807 missense variant C/G;T snv 4
rs397517071
ACTC1 ; LOC101928174
1.000 0.040 15 34792092 missense variant A/G snv 2
rs727503741
VCL
1.000 0.040 10 74114349 stop gained C/T snv 2
rs727504379
ACTC1 ; LOC101928174
1.000 0.040 15 34791238 missense variant A/G snv 2