rs397516881, BAG3

N. diseases: 5
Source: BEFREE ×
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
65 0.827 0.120 10 119676917 missense variant G/A snv 0.710 1.000 1 2011 2017
Cardiomyopathy, Familial Idiopathic
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
200 0.827 0.120 10 119676917 missense variant G/A snv 0.010 1.000 1 2017 2017
Congestive heart failure
CUI: C0018802
Disease: Congestive heart failure
156 0.827 0.120 10 119676917 missense variant G/A snv 0.010 1.000 1 2017 2017
Heart failure
CUI: C0018801
Disease: Heart failure
120 0.827 0.120 10 119676917 missense variant G/A snv 0.010 1.000 1 2017 2017
Myopathy
CUI: C0026848
Disease: Myopathy
93 0.827 0.120 10 119676917 missense variant G/A snv 0.010 1.000 1 2017 2017