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
rs12921862
AXIN1
0.763 0.200 16 331927 intron variant C/A snv 0.18 10
rs58034145
LMNA
0.827 0.160 1 156134830 missense variant A/C snv 10