rs267607578, LMNA

N. diseases: 3
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 0.925 0.120 1 156136952 missense variant G/A;C snv 1.4E-05 0.810 1.000 24 1999 2014
Hereditary Motor and Sensory-Neuropathy Type II
CUI: C0270914
Disease: Hereditary Motor and Sensory-Neuropathy Type II
144 0.925 0.120 1 156136952 missense variant G/A;C snv 1.4E-05 0.700 1.000 5 2007 2017
Cardiomyopathy, Dilated
CUI: C0007193
Disease: Cardiomyopathy, Dilated
509 0.925 0.120 1 156136952 missense variant G/A;C snv 1.4E-05 0.700 1.000 4 2007 2012