rs28933093, LMNA

N. diseases: 3
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 0.882 0.160 1 156130741 missense variant G/A snv 0.810 1.000 1 1999 2012
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
233 0.882 0.160 1 156130741 missense variant G/A snv 0.010 1.000 1 2003 2003
Myopathy
CUI: C0026848
Disease: Myopathy
93 0.882 0.160 1 156130741 missense variant G/A snv 0.010 1.000 1 2003 2003