rs146275785, NEBL

N. diseases: 3
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 10 20828531 missense variant G/A;T snv 7.2E-05; 2.7E-04 0.010 1.000 1 2010 2010
Cardiomyopathy, Familial Idiopathic
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
243 0.925 0.040 10 20828531 missense variant G/A;T snv 7.2E-05; 2.7E-04 0.010 1.000 1 2010 2010
Endocardial Fibroelastosis
CUI: C0014117
Disease: Endocardial Fibroelastosis
2 0.925 0.040 10 20828531 missense variant G/A;T snv 7.2E-05; 2.7E-04 0.010 1.000 1 2010 2010