rs61195471, 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 0.827 0.160 1 156134496 missense variant G/A snv 0.700 1.000 17 1999 2012
Hereditary Motor and Sensory-Neuropathy Type II
144 0.827 0.160 1 156134496 missense variant G/A snv 0.700 1.000 6 1999 2012
Cardiomyopathy, Dilated
CUI: C0007193
Disease: Cardiomyopathy, Dilated
509 0.827 0.160 1 156134496 missense variant G/A snv 0.700 1.000 5 2001 2013
Autosomal Dominant Emery-Dreifuss Muscular Dystrophy (disorder)
74 0.827 0.160 1 156134496 missense variant G/A snv 0.700 0
Congestive heart failure
CUI: C0018802
Disease: Congestive heart failure
165 0.827 0.160 1 156134496 missense variant G/A snv 0.010 1.000 1 2001 2001
Heart failure
CUI: C0018801
Disease: Heart failure
201 0.827 0.160 1 156134496 missense variant G/A snv 0.010 1.000 1 2001 2001