rs61661343, 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, Familial Idiopathic
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
243 0.851 0.040 1 156130687 missense variant T/C snv 0.720 1.000 18 1999 2019
Familial dilated cardiomyopathy
CUI: C0340427
Disease: Familial dilated cardiomyopathy
47 0.851 0.040 1 156130687 missense variant T/C snv 0.020 1.000 2 2004 2016
Congestive heart failure
CUI: C0018802
Disease: Congestive heart failure
165 0.851 0.040 1 156130687 missense variant T/C snv 0.010 1.000 1 2004 2004
Heart failure
CUI: C0018801
Disease: Heart failure
201 0.851 0.040 1 156130687 missense variant T/C snv 0.010 1.000 1 2004 2004