rs267607576, LMNA

N. diseases: 2
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.
Muscular Dystrophy
CUI: C0026850
Disease: Muscular Dystrophy
67 0.925 0.160 1 156136219 missense variant G/A;C snv 1.2E-05 0.700 0
Cardiomyopathy, Familial Idiopathic
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
243 0.925 0.160 1 156136219 missense variant G/A;C snv 1.2E-05 0.700 1.000 17 1999 2012