rs59270054, LMNA

N. diseases: 6
Source: ALL
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, Dilated
CUI: C0007193
Disease: Cardiomyopathy, Dilated
509 0.925 0.120 1 156115162 missense variant G/A;C snv 0.720 1.000 6 2005 2010
Hereditary Motor and Sensory-Neuropathy Type II
144 0.925 0.120 1 156115162 missense variant G/A;C snv 0.700 1.000 4 2006 2010
Cardiomyopathies
CUI: C0878544
Disease: Cardiomyopathies
294 0.925 0.120 1 156115162 missense variant G/A;C snv 0.010 1.000 1 2006 2006
Conduction disorder of the heart
CUI: C0264886
Disease: Conduction disorder of the heart
11 0.925 0.120 1 156115162 missense variant G/A;C snv 0.010 1.000 1 2006 2006
Familial dilated cardiomyopathy
CUI: C0340427
Disease: Familial dilated cardiomyopathy
47 0.925 0.120 1 156115162 missense variant G/A;C snv 0.010 1.000 1 2010 2010
Heart Diseases
CUI: C0018799
Disease: Heart Diseases
45 0.925 0.120 1 156115162 missense variant G/A;C snv 0.010 1.000 1 2010 2010