rs59301204, LMNA

N. diseases: 4
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 0.080 1 156135956 missense variant G/A;C snv 1.2E-05 0.710 1.000 9 2007 2018
Cardiomyopathies
CUI: C0878544
Disease: Cardiomyopathies
294 0.925 0.080 1 156135956 missense variant G/A;C snv 1.2E-05 0.700 0
Cardiomyopathy, Familial Idiopathic
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
243 0.925 0.080 1 156135956 missense variant G/A;C snv 1.2E-05 0.010 1.000 1 2017 2017
Ventricular arrhythmia
CUI: C0085612
Disease: Ventricular arrhythmia
37 0.925 0.080 1 156135956 missense variant G/A;C snv 1.2E-05 0.010 1.000 1 2017 2017