rs56793579, LMNA

N. diseases: 5
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.
Familial Partial Lipodystrophy, Type 2
CUI: C1720860
Disease: Familial Partial Lipodystrophy, Type 2
23 0.851 0.240 1 156115102 missense variant C/G;T snv 0.800 0
Cardiomyopathies
CUI: C0878544
Disease: Cardiomyopathies
294 0.851 0.240 1 156115102 missense variant C/G;T snv 0.710 1.000 3 2002 2010
Hereditary Motor and Sensory-Neuropathy Type II
CUI: C0270914
Disease: Hereditary Motor and Sensory-Neuropathy Type II
144 0.851 0.240 1 156115102 missense variant C/G;T snv 0.700 0
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
584 0.851 0.240 1 156115102 missense variant C/G;T snv 0.010 1.000 1 2010 2010
Congestive heart failure
CUI: C0018802
Disease: Congestive heart failure
165 0.851 0.240 1 156115102 missense variant C/G;T snv 0.010 1.000 1 2010 2010