rs59026483, LMNA

N. diseases: 7
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 156134457 missense variant C/T snv 7.0E-06 0.710 0.944 18 1999 2012
Hereditary Motor and Sensory-Neuropathy Type II
CUI: C0270914
Disease: Hereditary Motor and Sensory-Neuropathy Type II
144 0.827 0.160 1 156134457 missense variant C/T snv 7.0E-06 0.700 1.000 8 2002 2015
CARDIOMYOPATHY, DILATED, 1S
CUI: C1834481
Disease: CARDIOMYOPATHY, DILATED, 1S
53 0.827 0.160 1 156134457 missense variant C/T snv 7.0E-06 0.700 0
Cardiomyopathy, Dilated
CUI: C0007193
Disease: Cardiomyopathy, Dilated
509 0.827 0.160 1 156134457 missense variant C/T snv 7.0E-06 0.010 1.000 1 2004 2004
Familial dilated cardiomyopathy
CUI: C0340427
Disease: Familial dilated cardiomyopathy
47 0.827 0.160 1 156134457 missense variant C/T snv 7.0E-06 0.010 1.000 1 2007 2007
Left Ventricular Hypertrophy
CUI: C0149721
Disease: Left Ventricular Hypertrophy
67 0.827 0.160 1 156134457 missense variant C/T snv 7.0E-06 0.010 1.000 1 2008 2008
Myopathy
CUI: C0026848
Disease: Myopathy
166 0.827 0.160 1 156134457 missense variant C/T snv 7.0E-06 0.010 1.000 1 2005 2005