rs57045855, 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, Familial Idiopathic
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
243 0.882 0.040 1 156134464 missense variant A/G;T snv 0.720 1.000 18 1999 2012
Cardiomyopathies
CUI: C0878544
Disease: Cardiomyopathies
294 0.882 0.040 1 156134464 missense variant A/G;T snv 0.020 1.000 2 2010 2015
Cardiomyopathy, Dilated
CUI: C0007193
Disease: Cardiomyopathy, Dilated
509 0.882 0.040 1 156134464 missense variant A/G;T snv 0.010 1.000 1 2008 2008
Congestive heart failure
CUI: C0018802
Disease: Congestive heart failure
165 0.882 0.040 1 156134464 missense variant A/G;T snv 0.010 1.000 1 2006 2006
Heart failure
CUI: C0018801
Disease: Heart failure
201 0.882 0.040 1 156134464 missense variant A/G;T snv 0.010 1.000 1 2006 2006
Myopathy
CUI: C0026848
Disease: Myopathy
166 0.882 0.040 1 156134464 missense variant A/G;T snv 0.010 1.000 1 2015 2015