rs28933093, LMNA

N. diseases: 5
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, Familial Idiopathic
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
243 0.882 0.160 1 156130741 missense variant G/A snv 0.810 1.000 17 1999 2012
Cardiomyopathy, Dilated
CUI: C0007193
Disease: Cardiomyopathy, Dilated
509 0.882 0.160 1 156130741 missense variant G/A snv 0.700 1.000 4 2003 2009
Hereditary Motor and Sensory-Neuropathy Type II
144 0.882 0.160 1 156130741 missense variant G/A snv 0.700 1.000 3 2013 2018
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
584 0.882 0.160 1 156130741 missense variant G/A snv 0.010 1.000 1 2003 2003
Myopathy
CUI: C0026848
Disease: Myopathy
166 0.882 0.160 1 156130741 missense variant G/A snv 0.010 1.000 1 2003 2003