rs1739843, HSPB7

N. diseases: 4
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 0.882 0.040 1 16016759 intron variant T/C snv 0.62 0.700 1.000 1 2010 2010
Cardiomyopathy, Familial Idiopathic
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
243 0.882 0.040 1 16016759 intron variant T/C snv 0.62 0.030 1.000 3 2010 2016
Congestive heart failure
CUI: C0018802
Disease: Congestive heart failure
165 0.882 0.040 1 16016759 intron variant T/C snv 0.62 0.010 1.000 1 2010 2010
Heart failure
CUI: C0018801
Disease: Heart failure
201 0.882 0.040 1 16016759 intron variant T/C snv 0.62 0.010 1.000 1 2010 2010