rs28933092, 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.
Cardiomyopathy, Familial Idiopathic
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
243 1.000 0.040 1 156134497 missense variant A/G;T snv 0.800 1.000 17 1999 2012
Cardiomyopathy, Dilated
CUI: C0007193
Disease: Cardiomyopathy, Dilated
509 1.000 0.040 1 156134497 missense variant A/G;T snv 0.700 1.000 4 1999 2008