rs56984562, 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 0.827 0.200 1 156137666 missense variant C/A;G;T snv 0.810 1.000 1 1999 2017
Dyskinetic syndrome
CUI: C0013384
Disease: Dyskinetic syndrome
29 0.827 0.200 1 156137666 missense variant C/A;G;T snv 0.010 1.000 1 2011 2011
Ventricular arrhythmia
CUI: C0085612
Disease: Ventricular arrhythmia
34 0.827 0.200 1 156137666 missense variant C/A;G;T snv 0.010 1.000 1 2010 2010