Disease: Cardiomyopathy, Familial Idiopathic
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs153109
IL27
0.623 0.600 16 28507775 intron variant T/C snv 0.43 37
rs1801253
ADRB1
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 34
rs1801252
ADRB1
0.724 0.320 10 114044277 missense variant A/G snv 0.15 0.17 17
rs1805124
SCN5A
0.742 0.280 3 38603929 missense variant T/C snv 0.22 0.25 16
rs61672878
LMNA
0.776 0.200 1 156136094 missense variant G/A;T snv 11
rs3745297
HRC
0.790 0.120 19 49154952 missense variant A/C snv 0.41 0.38 10
rs28933093
LMNA
0.882 0.160 1 156130741 missense variant G/A snv 5
rs58672172
LMNA
0.882 0.160 1 156136251 missense variant C/T snv 1.2E-05 1.4E-05 3