rs1553265736, 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, Dilated
CUI: C0007193
Disease: Cardiomyopathy, Dilated
509 0.925 0.040 1 156136080 missense variant G/C snv 0.700 0
Cardiomyopathy, Familial Idiopathic
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
243 0.925 0.040 1 156136080 missense variant G/C snv 0.700 0
Congestive heart failure
CUI: C0018802
Disease: Congestive heart failure
165 0.925 0.040 1 156136080 missense variant G/C snv 0.700 0
Electrocardiogram change
CUI: C0855329
Disease: Electrocardiogram change
27 0.925 0.040 1 156136080 missense variant G/C snv 0.700 0