rs201583907, 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 0.925 0.040 1 156137191 missense variant G/A;C snv 8.6E-05 0.700 1.000 17 1999 2012
Left ventricular noncompaction
CUI: C1960469
Disease: Left ventricular noncompaction
26 0.925 0.040 1 156137191 missense variant G/A;C snv 8.6E-05 0.700 0