rs59026483, LMNA

N. diseases: 5
Source: BEFREE ×
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Cardiomyopathy, Familial Idiopathic
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
200 0.827 0.160 1 156134457 missense variant C/T snv 7.0E-06 0.710 0.944 1 1999 2012
Cardiomyopathy, Dilated
CUI: C0007193
Disease: Cardiomyopathy, Dilated
65 0.827 0.160 1 156134457 missense variant C/T snv 7.0E-06 0.010 1.000 1 2004 2004
Familial dilated cardiomyopathy
CUI: C0340427
Disease: Familial dilated cardiomyopathy
15 0.827 0.160 1 156134457 missense variant C/T snv 7.0E-06 0.010 1.000 1 2007 2007
Left Ventricular Hypertrophy
CUI: C0149721
Disease: Left Ventricular Hypertrophy
57 0.827 0.160 1 156134457 missense variant C/T snv 7.0E-06 0.010 1.000 1 2008 2008
Myopathy
CUI: C0026848
Disease: Myopathy
93 0.827 0.160 1 156134457 missense variant C/T snv 7.0E-06 0.010 1.000 1 2005 2005