rs397516881, BAG3

N. diseases: 7
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, 1HH
CUI: C3151293
Disease: CARDIOMYOPATHY, DILATED, 1HH
21 0.827 0.120 10 119676917 missense variant G/A snv 0.800 1.000 5 1990 2014
Cardiomyopathy, Dilated
CUI: C0007193
Disease: Cardiomyopathy, Dilated
509 0.827 0.120 10 119676917 missense variant G/A snv 0.710 1.000 4 2011 2017
Myopathy, Myofibrillar, Bag3-Related
CUI: C2751831
Disease: Myopathy, Myofibrillar, Bag3-Related
11 0.827 0.120 10 119676917 missense variant G/A snv 0.700 1.000 2 1990 2014
Cardiomyopathy, Familial Idiopathic
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
243 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
165 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
201 0.827 0.120 10 119676917 missense variant G/A snv 0.010 1.000 1 2017 2017
Myopathy
CUI: C0026848
Disease: Myopathy
166 0.827 0.120 10 119676917 missense variant G/A snv 0.010 1.000 1 2017 2017